FDA 510(k)

SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023

K-Number: K041453 · 2004-07-22

Decision Date2004-07-22

Product CodeDWQ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2004-07-22 under 510(k) number K041453. 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 SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023?

SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 is a medical device that received FDA 510(k) clearance on 2004-07-22. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K041453.

When did SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 receive FDA 510(k) clearance?

SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 received FDA 510(k) clearance on 2004-07-22, under 510(k) number K041453.

Who is the listed applicant for SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023?

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

What is the FDA product code for SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023?

The FDA product code for SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 is DWQ.

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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.