SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED— 510(k) K892522

Name: FDA 510(k) clearance K892522
Creator: U.S. Food and Drug Administration
Published: 1989-05-24

Substantially Equivalent

Gespac, Inc.

FDA 510(k) clearance K892522 for SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED, Substantially Equivalent on 1989-05-24. 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: 1989-04-11
Decision date: 1989-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

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Recent devices under product code GKB

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K890503 — SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE1989-02-10

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