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FDA 510(k)

VEIN-TRAP TM

K-Number: K811910 · 1981-07-20

ApplicantAtrium Medical Corp.
Decision Date1981-07-20
Product CodeDWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VEIN-TRAP TM is the device name listed in this FDA 510(k) record. The listed applicant is Atrium Medical Corp.. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811910. The device is classified under product code DWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEIN-TRAP TM?

VEIN-TRAP TM is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Atrium Medical Corp.. The 510(k) number is K811910.

When did VEIN-TRAP TM receive FDA 510(k) clearance?

VEIN-TRAP TM received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811910.

Who is the listed applicant for VEIN-TRAP TM?

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

What is the FDA product code for VEIN-TRAP TM?

The FDA product code for VEIN-TRAP TM is DWQ.

Other records listing Atrium Medical 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.

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Related Devices (Code: DWQ)

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.

K212894PhasTIPPLeMaitre Vascular, Inc.K041453SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023Smith & Nephew, Inc.K032387TRIVEX SYSTEMSmith & Nephew, Inc.K905528URESIL VALVE CUTTERUresil Corp.K904507PILLING BRUSH VALVULOTOMEPilling Co.K885046INSITUCAT VALVE STRIPPERAesculap Instruments Corp.

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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