510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K812836Unknown

Ldh Reagent Set

Anco Medical Reagents & Assoc., Mchenry IL / Traditional, Unknown
FDA source (opens on fda.gov)

K812836 is the FDA 510(k) clearance record for LDH REAGENT SET, a class II device, cleared for Anco Medical Reagents & Assoc. on under FDA product code CFH (Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase). FDA records list 26 510(k) clearances for Anco Medical Reagents & Assoc., from to . As of , FDA records show no recalls naming K812836.

Clearance record

Decision date
Received
(0 days to decision)
Product code
CFH Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase
Regulation
21 CFR 862.1440
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Anco Medical Reagents & Assoc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CFH

Trailing 12 months

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

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