SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE— 510(k) K890503

Name: FDA 510(k) clearance K890503
Creator: U.S. Food and Drug Administration
Published: 1989-02-10

Substantially Equivalent

Gespac, Inc.

FDA 510(k) clearance K890503 for SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE, Substantially Equivalent on 1989-02-10. Applicant: Gespac, Inc.. Device class: 1.

Clearance details

Applicant: Gespac, Inc.
Product code: Code GKB
Device class: Class 1
Regulation: 21 CFR 864.5800
Advisory panel: Hematology
Date received: 1989-02-01
Decision date: 1989-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

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