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FDA 510(k)

HEMO-BARRIER TOURNIQUET

K-Number: K950258 · 1995-06-19

ApplicantHemo-Barrier Technologies, Inc.
Decision Date1995-06-19
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

HEMO-BARRIER TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Hemo-Barrier Technologies, Inc.. It received FDA 510(k) clearance on 1995-06-19 under 510(k) number K950258. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMO-BARRIER TOURNIQUET?

HEMO-BARRIER TOURNIQUET is a medical device that received FDA 510(k) clearance on 1995-06-19. The listed applicant is Hemo-Barrier Technologies, Inc.. The 510(k) number is K950258.

When did HEMO-BARRIER TOURNIQUET receive FDA 510(k) clearance?

HEMO-BARRIER TOURNIQUET received FDA 510(k) clearance on 1995-06-19, under 510(k) number K950258.

Who is the listed applicant for HEMO-BARRIER TOURNIQUET?

The FDA 510(k) record lists Hemo-Barrier Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMO-BARRIER TOURNIQUET?

The FDA product code for HEMO-BARRIER TOURNIQUET is EFQ.

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Related Devices (Code: EFQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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