RELLPLATE C KIT, RELLPLATE C BULK PLATES— 510(k) K884940

Name: FDA 510(k) clearance K884940
Creator: U.S. Food and Drug Administration
Published: 1989-03-13

Substantially Equivalent

American Diagnostic Corp.

FDA 510(k) clearance K884940 for RELLPLATE C KIT, RELLPLATE C BULK PLATES, Substantially Equivalent on 1989-03-13. Applicant: American Diagnostic Corp.. Device class: 2.

Clearance details

Applicant: American Diagnostic Corp.
Product code: Code GGP
Device class: Class 2
Regulation: 21 CFR 864.7290
Advisory panel: Hematology
Date received: 1988-11-28
Decision date: 1989-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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