510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792551Substantially Equivalent

Alkaline Phosphatase Reagent

Electrophoresis Corp. of America, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792551 is the FDA 510(k) clearance record for ALKALINE PHOSPHATASE REAGENT, a class II device, cleared for Electrophoresis Corp. of America on under FDA product code CJH (Thymol Blue Monophosphate, Alkaline Phosphatase Or Isoenzymes). FDA records list 27 510(k) clearances for Electrophoresis Corp. of America, from to . As of , FDA records show no recalls naming K792551.

Clearance record

Decision date
Received
(50 days to decision)
Product code
CJH Thymol Blue Monophosphate, Alkaline Phosphatase Or Isoenzymes
Regulation
21 CFR 862.1050
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Electrophoresis Corp. of America 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code CJH

Trailing 12 months

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

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