Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K053612Substantially Equivalent

Dri-Stat Acid Phosphatase Reagent

Siemens Healthcare Diagnostics Inc., Brea CA / Traditional, Substantially Equivalent

K053612 is the FDA 510(k) clearance record for DRI-STAT ACID PHOSPHATASE REAGENT, a class II device, cleared for Beckman Coulter, Inc. on under FDA product code CKB (Acid Phosphatase, Naphthyl Phosphate). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K053612.

Clearance record

Decision date
Received
(120 days to decision)
Product code
CKB Acid Phosphatase, Naphthyl Phosphate
Regulation
21 CFR 862.1020
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Beckman Coulter, Inc. 200 S. Kraemer Blvd. W-110, Brea CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CKB

Trailing 12 months

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

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