HEMO-BARRIER TOURNIQUET— 510(k) K950258

Name: FDA 510(k) clearance K950258
Creator: U.S. Food and Drug Administration
Published: 1995-06-19

Substantially Equivalent

Hemo-Barrier Technologies, Inc.

FDA 510(k) clearance K950258 for HEMO-BARRIER TOURNIQUET, Substantially Equivalent on 1995-06-19. Applicant: Hemo-Barrier Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Hemo-Barrier Technologies, Inc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-01-23
Decision date: 1995-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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