Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K760397Substantially Equivalent

Reagent, Amp Buffer Diagnostic

J.T. Baker Chemical Co., Mchenry IL / Traditional, Substantially Equivalent

K760397 is the FDA 510(k) clearance record for REAGENT, AMP BUFFER DIAGNOSTIC, a class II device, cleared for J.T. Baker Chemical Co. on under FDA product code CJE (Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes). FDA records list 54 510(k) clearances for J.T. Baker Chemical Co., from to . As of , FDA records show no recalls naming K760397.

Clearance record

Decision date
Received
(87 days to decision)
Product code
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
Regulation
21 CFR 862.1050
Device class
Class II
Review panel
Clinical Chemistry
Applicant
J.T. Baker Chemical Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CJE

Trailing 12 months
1 clearance under product code CJE in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CJE, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260