Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K880798Substantially Equivalent

Acid Phosphatase Reagent

Trace America, Inc., Miami FL / Traditional, Substantially Equivalent

K880798 is the FDA 510(k) clearance record for ACID PHOSPHATASE REAGENT, a class II device, cleared for Trace America, Inc. on under FDA product code CKB (Acid Phosphatase, Naphthyl Phosphate). FDA records list 22 510(k) clearances for Trace America, Inc., from to . As of , FDA records show no recalls naming K880798.

Clearance record

Decision date
Received
(52 days to decision)
Product code
CKB Acid Phosphatase, Naphthyl Phosphate
Regulation
21 CFR 862.1020
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Trace America, Inc. P.O. Box 45-1835, Miami FL
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