510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K863851Substantially Equivalent

Acid Phosphatase (Acp) Reagent

Sigma Diagnostics, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863851 is the FDA 510(k) clearance record for ACID PHOSPHATASE (ACP) REAGENT, a class II device, cleared for Sigma Diagnostics, Inc. on under FDA product code CKB (Acid Phosphatase, Naphthyl Phosphate). FDA records list 164 510(k) clearances for Sigma Diagnostics, Inc., from to . As of , FDA records show no recalls naming K863851.

Clearance record

Decision date
Received
(14 days to decision)
Product code
CKB Acid Phosphatase, Naphthyl Phosphate
Regulation
21 CFR 862.1020
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Sigma Diagnostics, Inc. P.O. Box 14508, St. Louis MO
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