510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K813244Substantially Equivalent

UV Uric Acid Determination

Biorent Diagnostic, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K813244 is the FDA 510(k) clearance record for UV URIC ACID DETERMINATION, a class I device, cleared for Biorent Diagnostic, Inc. on under FDA product code CDO (Acid, Uric, Uricase (U.V.)). FDA records list 11 510(k) clearances for Biorent Diagnostic, Inc., from to . As of , FDA records show no recalls naming K813244.

Clearance record

Decision date
Received
(20 days to decision)
Product code
CDO Acid, Uric, Uricase (U.V.)
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Biorent Diagnostic, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CDO

Trailing 12 months

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

FDA records show no clearances under product code CDO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CDO, 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