510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834033Substantially Equivalent

Kinetic Alkaline Phosphatase

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

K834033 is the FDA 510(k) clearance record for KINETIC ALKALINE PHOSPHATASE, a class II device, cleared for American Monitor Corp. on under FDA product code CJE (Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes). FDA records list 73 510(k) clearances for American Monitor Corp., from to . As of , FDA records show no recalls naming K834033.

Clearance record

Decision date
Received
(68 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
American Monitor Corp. 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