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
K771605Substantially Equivalent

Creatine Kinase Isoenzyme Substrate Set

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

K771605 is the FDA 510(k) clearance record for CREATINE KINASE ISOENZYME SUBSTRATE SET, a class II device, cleared for Pfizer Pharmaceuticals on under FDA product code JHX (Fluorometric Method, Cpk Or Isoenzymes). FDA records list 6 510(k) clearances for Pfizer Pharmaceuticals, from to . As of , FDA records show no recalls naming K771605.

Clearance record

Decision date
Received
(24 days to decision)
Product code
JHX Fluorometric Method, Cpk Or Isoenzymes
Regulation
21 CFR 862.1215
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Pfizer Pharmaceuticals 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JHX

Trailing 12 months

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

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