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FDA 510(k)

ESSAR TOURNIQUET FOR VENIPUNCTURE

K-Number: K790802 · 1979-05-01

ApplicantStewart Research, Inc.
Decision Date1979-05-01
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ESSAR TOURNIQUET FOR VENIPUNCTURE is the device name listed in this FDA 510(k) record. The listed applicant is Stewart Research, Inc.. It received FDA 510(k) clearance on 1979-05-01 under 510(k) number K790802. 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 ESSAR TOURNIQUET FOR VENIPUNCTURE?

ESSAR TOURNIQUET FOR VENIPUNCTURE is a medical device that received FDA 510(k) clearance on 1979-05-01. The listed applicant is Stewart Research, Inc.. The 510(k) number is K790802.

When did ESSAR TOURNIQUET FOR VENIPUNCTURE receive FDA 510(k) clearance?

ESSAR TOURNIQUET FOR VENIPUNCTURE received FDA 510(k) clearance on 1979-05-01, under 510(k) number K790802.

Who is the listed applicant for ESSAR TOURNIQUET FOR VENIPUNCTURE?

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

What is the FDA product code for ESSAR TOURNIQUET FOR VENIPUNCTURE?

The FDA product code for ESSAR TOURNIQUET FOR VENIPUNCTURE 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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