QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM— 510(k) K972969

Name: FDA 510(k) clearance K972969
Creator: U.S. Food and Drug Administration
Published: 1997-09-22

Substantially Equivalent

Innovative Medical Technologies, Inc.

FDA 510(k) clearance K972969 for QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM, Substantially Equivalent on 1997-09-22. Applicant: Innovative Medical Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Innovative Medical Technologies, Inc.
Product code: Code GIO
Device class: Class 1
Regulation: 21 CFR 864.6150
Advisory panel: Hematology
Date received: 1997-08-11
Decision date: 1997-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

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