510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K820722Substantially Equivalent

Kodak Ektachem Clinical Chemistry Slidde

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

K820722 is the FDA 510(k) clearance record for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDDE, a class II device, cleared for Eastman Kodak Company on under FDA product code JHS (Differential Rate Kinetic Method, Cpk Or Isoenzymes). FDA records list 291 510(k) clearances for Eastman Kodak Company, from to . As of , FDA records show no recalls naming K820722.

Clearance record

Decision date
Received
(16 days to decision)
Product code
JHS Differential Rate Kinetic Method, Cpk Or Isoenzymes
Regulation
21 CFR 862.1215
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Eastman Kodak Company 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JHS

Trailing 12 months

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

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