510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K914167Substantially Equivalent

Clinical Chem.anal.acid,prostatic Acid Phosphatase

Eastman Kodak Company, Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914167 is the FDA 510(k) clearance record for CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASE, a class II device, cleared for Eastman Kodak Company on under FDA product code CKE (Acid Phosphatase, Thymolphthale Inmonophosphate). FDA records list 291 510(k) clearances for Eastman Kodak Company, from to . As of , FDA records show no recalls naming K914167.

Clearance record

Decision date
Received
(182 days to decision)
Product code
CKE Acid Phosphatase, Thymolphthale Inmonophosphate
Regulation
21 CFR 862.1020
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Eastman Kodak Company 343 State St., Rochester NY
510(k) summary
Statement
Third party review
No

Clearances, product code CKE

Trailing 12 months

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

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