510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890312Substantially Equivalent

Gamma-Glutamyltransferase

American Monitor Corp., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890312 is the FDA 510(k) clearance record for GAMMA-GLUTAMYLTRANSFERASE, a class I device, cleared for American Monitor Corp. on under FDA product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase). FDA records list 73 510(k) clearances for American Monitor Corp., from to . As of , FDA records show no recalls naming K890312.

Clearance record

Decision date
Received
(60 days to decision)
Product code
JQB Kinetic Method, Gamma-Glutamyl Transpeptidase
Regulation
21 CFR 862.1360
Device class
Class I
Review panel
Clinical Chemistry
Applicant
American Monitor Corp. P.O. Box 68505, Indianapolis IN
Third party review
No

Clearances, product code JQB

Trailing 12 months

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

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