HEMOCHEK-A1C SAMPLE COLLECTION KIT— 510(k) K990899

Name: FDA 510(k) clearance K990899
Creator: U.S. Food and Drug Administration
Published: 1999-12-21

Substantially Equivalent

Osborn Group, Inc.

FDA 510(k) clearance K990899 for HEMOCHEK-A1C SAMPLE COLLECTION KIT, Substantially Equivalent on 1999-12-21. Applicant: Osborn Group, Inc.. Device class: 2.

Clearance details

Applicant: Osborn Group, Inc.
Product code: Code LCP
Device class: Class 2
Regulation: 21 CFR 864.7470
Advisory panel: Hematology
Date received: 1999-03-18
Decision date: 1999-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Olathe, KS, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.