KODAK SURECELL CHLAMYDIA TEST KIT— 510(k) K882923

Name: FDA 510(k) clearance K882923
Creator: U.S. Food and Drug Administration
Published: 1988-11-10

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K882923 for KODAK SURECELL CHLAMYDIA TEST KIT, Substantially Equivalent on 1988-11-10. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LJC
Device class: Class 1
Regulation: 21 CFR 866.3120
Advisory panel: Microbiology
Date received: 1988-07-13
Decision date: 1988-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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