FDA 510(k)

SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273

K-Number: K012724 · 2001-11-08

Decision Date2001-11-08

Product CodeLYK

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273 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 2001-11-08 under 510(k) number K012724. The device is classified under product code LYK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273?

SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273 is a medical device that received FDA 510(k) clearance on 2001-11-08. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K012724.

When did SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273 receive FDA 510(k) clearance?

SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273 received FDA 510(k) clearance on 2001-11-08, under 510(k) number K012724.

Who is the listed applicant for SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273?

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 VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273?

The FDA product code for SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273 is LYK.

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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.