510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K771343Substantially Equivalent

Ldh-Int Test

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

K771343 is the FDA 510(k) clearance record for LDH-INT TEST, a class II device, cleared for Hycel, Inc. on under FDA product code CFH (Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase). FDA records list 19 510(k) clearances for Hycel, Inc., from to . As of , FDA records show no recalls naming K771343.

Clearance record

Decision date
Received
(21 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
Hycel, Inc. 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