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FDA 510(k)

LQUET CANNULA/TROCAR SYSTEM

K-Number: K974139 · 1998-01-28

ApplicantLifequest Endoscopic Technologies, Inc.
Decision Date1998-01-28
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LQUET CANNULA/TROCAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lifequest Endoscopic Technologies, Inc.. It received FDA 510(k) clearance on 1998-01-28 under 510(k) number K974139. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LQUET CANNULA/TROCAR SYSTEM?

LQUET CANNULA/TROCAR SYSTEM is a medical device that received FDA 510(k) clearance on 1998-01-28. The listed applicant is Lifequest Endoscopic Technologies, Inc.. The 510(k) number is K974139.

When did LQUET CANNULA/TROCAR SYSTEM receive FDA 510(k) clearance?

LQUET CANNULA/TROCAR SYSTEM received FDA 510(k) clearance on 1998-01-28, under 510(k) number K974139.

Who is the listed applicant for LQUET CANNULA/TROCAR SYSTEM?

The FDA 510(k) record lists Lifequest Endoscopic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LQUET CANNULA/TROCAR SYSTEM?

The FDA product code for LQUET CANNULA/TROCAR SYSTEM is GCJ.

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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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