510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850933Substantially Equivalent

Uric Acid

Dilab, Inc., Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850933 is the FDA 510(k) clearance record for URIC ACID, a class I device, cleared for Dilab, Inc. on under FDA product code CDH (Acid, Uric, Phosphotungstate Reduction). FDA records list 11 510(k) clearances for Dilab, Inc., from to . As of , FDA records show no recalls naming K850933.

Clearance record

Decision date
Received
(110 days to decision)
Product code
CDH Acid, Uric, Phosphotungstate Reduction
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Dilab, Inc. 7003 NW 50th St., Miami FL
Third party review
No

Clearances, product code CDH

Trailing 12 months

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

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