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FDA 510(k)

INSTRUMENTS FOR LAPAROSCOPIC USE

K-Number: K931142 · 1993-06-25

Decision Date1993-06-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENTS FOR LAPAROSCOPIC USE is the device name listed in this FDA 510(k) record. The listed applicant is Li Medical Technologies, Inc.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K931142. 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 INSTRUMENTS FOR LAPAROSCOPIC USE?

INSTRUMENTS FOR LAPAROSCOPIC USE is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is Li Medical Technologies, Inc.. The 510(k) number is K931142.

When did INSTRUMENTS FOR LAPAROSCOPIC USE receive FDA 510(k) clearance?

INSTRUMENTS FOR LAPAROSCOPIC USE received FDA 510(k) clearance on 1993-06-25, under 510(k) number K931142.

Who is the listed applicant for INSTRUMENTS FOR LAPAROSCOPIC USE?

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

What is the FDA product code for INSTRUMENTS FOR LAPAROSCOPIC USE?

The FDA product code for INSTRUMENTS FOR LAPAROSCOPIC USE is GCJ.

Related Clinical Trials

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.

Other records listing Li Medical Technologies, Inc. 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.

View all 17 devices →

Related Devices (Code: GCJ)

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.

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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