510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K063520Substantially Equivalent

Roche Total Mycophenolic Acid Assay, Calibrators and Controls

Roche Diagnostics GmbH, Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K063520 is the FDA 510(k) clearance record for ROCHE TOTAL MYCOPHENOLIC ACID ASSAY, CALIBRATORS AND CONTROLS, a class II device, cleared for Roche Diagnostics on under FDA product code OAV (Mycophenolic Acid Test System). FDA's definition for product code OAV reads: "An in vitro diagnostic reagent system intended for use in the quantitative determination of total mycophenolic acid in human serum or plasma as an aid in the management of mycophenolic acid therapy in renal and cardiac transplant patients". FDA records list 465 510(k) clearances for Roche Diagnostics, from to . As of , FDA records show no recalls naming K063520.

Clearance record

Decision date
Received
(87 days to decision)
Product code
OAV Mycophenolic Acid Test System
Regulation
21 CFR 862.3840
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Roche Diagnostics 9115 Hague Rd., Indianapolis IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OAV

Trailing 12 months

FDA records hold no clearances under product code OAV in the trailing twelve months.

FDA records show no clearances under product code OAV in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OAV, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260