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FDA 510(k)

TOURNEQUET, NON-PNEUMATIC

K-Number: K780429 · 1978-04-18

ApplicantHemox, Inc.
Decision Date1978-04-18
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TOURNEQUET, NON-PNEUMATIC is the device name listed in this FDA 510(k) record. The listed applicant is Hemox, Inc.. It received FDA 510(k) clearance on 1978-04-18 under 510(k) number K780429. The device is classified under product code GAX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOURNEQUET, NON-PNEUMATIC?

TOURNEQUET, NON-PNEUMATIC is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is Hemox, Inc.. The 510(k) number is K780429.

When did TOURNEQUET, NON-PNEUMATIC receive FDA 510(k) clearance?

TOURNEQUET, NON-PNEUMATIC received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780429.

Who is the listed applicant for TOURNEQUET, NON-PNEUMATIC?

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

What is the FDA product code for TOURNEQUET, NON-PNEUMATIC?

The FDA product code for TOURNEQUET, NON-PNEUMATIC is GAX.

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Related Devices (Code: GAX)

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.

K931198UNIQUETIcat SystemsK881398TOURNIQUETBarretta Products, Research and Development, Inc.K881176STERILE ESMARCH BANDAGESpectrum/Hydro-Med Products, Inc.K875092DEGANIA SILICONE TOURNIQUETDegania Silicone , Ltd.K873928UNIVERSAL TOURNIQUETDryden Corp.K872003KINDERWRAPThe Kinder Co.

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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