Eight one zero zero two was modifier 25 medicating Aetna are denying our urinalysis eight one two eight one two zero zero two stating that they are included with the office visit would it be appropriate to bill it with a modifier 25 well I found some really interesting information on this and you like my little urinalysis cup thought that was I really enjoy doing these slides but I also enjoy going and finding the pictures okay scrolling down so she got a similar question that I found on this in this article and the difference was it was too specific cousin says we received in the vials for Medicare for CPT code eight one zero zero two a urinalysis by dipstick or tablet reagent for Bella Reuben glucose hemoglobin ketones leukocytes nitrates pH protein specific event gravity gyro diligent any number of these constituents constituents constituents constituents okay I thought that was like a political thing I've not automated without microphones to Mike yeah okay and then she also had and the cpt code eight to two seven zero which is a blood occult that they'd won for feces to check for like colorectal cancer so the remittance code indicates that we must submit a modifier however we can't determine the appropriate modifier to report can you not give us any advice and she sure does so the answer she gave was when the physician's office performs this test in house you use modifier 92 alternative laboratory platform testing may be applicable the Hicks fixed modifier would be QW clinical laboratory Improvement Act waived test you could also use that so when the physician's office employs an outside laboratory to perform the tests you would report it with modifier ninety laboratory now if this is not the first...
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Clia Certification lookup Form: What You Should Know
The CIA Inspection Certificate (Form CMS-116) is valid for three years (12 months) and the certificate is renewable, subject to renewal. When renewing the inspection certificate, it is a requirement to provide information to the Department of Public Health to ensure that all laboratories are compliant with ISO and California standards. Sep 24, 2022 — Resources: FDA CIA's Cloning/Cloning/Cloning (DC/CL) Act Mar 23, 2022 — Resources: FDA's Cloning and Cloning (DC/CL) Act CERTIFICATE REQUIRED (i) Must be for a facility or establishment with at least 3,000 square feet of space where testing is being performed to verify the identity of laboratory personnel, and (ii) must verify that lab personnel are trained to perform laboratory tests as required under the CIA and are knowledgeable about the specific testing used to determine the existence of transmissible agent. (iii) Must ensure testing to determine the presence or absence of transmissible agents is to be performed on the most sensitive laboratory test instrument(s) and the most suitable solution, and that the information obtained is used only for the purpose described. (iv) All laboratory personnel performing testing must have valid CIA credentials or certification to perform laboratory tests and must perform the specific tests listed under the relevant section of the cloning act of 1988. (v) No information obtained by a facility or testing organization under this section is to be used for any purpose other than the specific purpose specified in this section. (vi) No information obtained will be used for any purpose other than to determine whether a facility is following the requirements of this act. (vii) The laboratory inspection will only be performed in accordance with the cloning act of 1988. (a) The inspection can happen at any time during the year, as required by the testing facility/ facility operator or the lab facility/ facility operator. (b) The inspection may happen at the location if the test is being conducted only at or near that location.
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