510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K820723Substantially Equivalent

Kodak Ektachem Clinical Chem. Nh3

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

K820723 is the FDA 510(k) clearance record for KODAK EKTACHEM CLINICAL CHEM. NH3, a class I device, cleared for Eastman Kodak Company on under FDA product code JID (Photometric Method, Ammonia). FDA records list 291 510(k) clearances for Eastman Kodak Company, from to . As of , FDA records show one recall naming K820723.

Clearance record

Decision date
Received
(16 days to decision)
Product code
JID Photometric Method, Ammonia
Regulation
21 CFR 862.1065
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Eastman Kodak Company 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JID

Trailing 12 months
1 clearance under product code JID in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JID, 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 20261
October 20260