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FDA 510(k)

TOURNIQUET

K-Number: K851482 · 1985-04-29

ApplicantPolymer Technology Corp.
Decision Date1985-04-29
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Polymer Technology Corp.. It received FDA 510(k) clearance on 1985-04-29 under 510(k) number K851482. 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 TOURNIQUET?

TOURNIQUET is a medical device that received FDA 510(k) clearance on 1985-04-29. The listed applicant is Polymer Technology Corp.. The 510(k) number is K851482.

When did TOURNIQUET receive FDA 510(k) clearance?

TOURNIQUET received FDA 510(k) clearance on 1985-04-29, under 510(k) number K851482.

Who is the listed applicant for TOURNIQUET?

The FDA 510(k) record lists Polymer Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOURNIQUET?

The FDA product code for TOURNIQUET is GAX.

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Other records listing Polymer Technology Corp. as applicant

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.

K011945RIGID GAS PERMEABLE CONTACT LENS SOLUTIONK980133BAUSCH & LOMB WETTING AND SOAKING SOLUTIONK974466BOSTON ADVANCE CLEANERK973217BOSTON LIQUID ENZYMATIC CLEANERK970698BOSTON ES MULTIVISION (ENFLUFOCON A) CONTACT LENSK951552BOSTON CONTACT LENS CASE

View all 23 devices →

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

View on FDA Database →

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

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