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FDA 510(k)

DEGANIA SILICONE TOURNIQUET

K-Number: K875092 · 1988-01-07

ApplicantDegania Silicone , Ltd.
Decision Date1988-01-07
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEGANIA SILICONE TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Degania Silicone , Ltd.. It received FDA 510(k) clearance on 1988-01-07 under 510(k) number K875092. 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 DEGANIA SILICONE TOURNIQUET?

DEGANIA SILICONE TOURNIQUET is a medical device that received FDA 510(k) clearance on 1988-01-07. The listed applicant is Degania Silicone , Ltd.. The 510(k) number is K875092.

When did DEGANIA SILICONE TOURNIQUET receive FDA 510(k) clearance?

DEGANIA SILICONE TOURNIQUET received FDA 510(k) clearance on 1988-01-07, under 510(k) number K875092.

Who is the listed applicant for DEGANIA SILICONE TOURNIQUET?

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

What is the FDA product code for DEGANIA SILICONE TOURNIQUET?

The FDA product code for DEGANIA SILICONE TOURNIQUET is GAX.

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Related Devices (Code: GAX)

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K931198UNIQUETIcat SystemsK881398TOURNIQUETBarretta Products, Research and Development, Inc.K881176STERILE ESMARCH BANDAGESpectrum/Hydro-Med Products, Inc.K873928UNIVERSAL TOURNIQUETDryden Corp.K872003KINDERWRAPThe Kinder Co.K864897DALE VENIPUNCTURE TOURNIQUET, PRODUCT NO. 1335Dale Medical Products, Inc.

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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