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FDA 510(k)

FINGER TOURNIQUETTE

K-Number: K853472 · 1985-10-10

ApplicantJoseph B. Marogil
Decision Date1985-10-10
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FINGER TOURNIQUETTE is the device name listed in this FDA 510(k) record. The listed applicant is Joseph B. Marogil. It received FDA 510(k) clearance on 1985-10-10 under 510(k) number K853472. 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 FINGER TOURNIQUETTE?

FINGER TOURNIQUETTE is a medical device that received FDA 510(k) clearance on 1985-10-10. The listed applicant is Joseph B. Marogil. The 510(k) number is K853472.

When did FINGER TOURNIQUETTE receive FDA 510(k) clearance?

FINGER TOURNIQUETTE received FDA 510(k) clearance on 1985-10-10, under 510(k) number K853472.

Who is the listed applicant for FINGER TOURNIQUETTE?

The FDA 510(k) record lists Joseph B. Marogil as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FINGER TOURNIQUETTE?

The FDA product code for FINGER TOURNIQUETTE is GAX.

Related Clinical Trials

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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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