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FDA 510(k)

LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE

K-Number: K022686 · 2002-11-25

ApplicantLap Surgical Systems, LLC
Decision Date2002-11-25
Product CodeFED
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Lap Surgical Systems, LLC. It received FDA 510(k) clearance on 2002-11-25 under 510(k) number K022686. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE?

LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE is a medical device that received FDA 510(k) clearance on 2002-11-25. The listed applicant is Lap Surgical Systems, LLC. The 510(k) number is K022686.

When did LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE receive FDA 510(k) clearance?

LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE received FDA 510(k) clearance on 2002-11-25, under 510(k) number K022686.

Who is the listed applicant for LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE?

The FDA 510(k) record lists Lap Surgical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE?

The FDA product code for LAP SURGICAL SYSTEMS MULTIPLE INSTRUMENT GUIDE is FED.

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Related Devices (Code: FED)

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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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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