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FDA 510(k)

LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS

K-Number: K925499 · 1994-02-18

ApplicantLapsurg of America
Decision Date1994-02-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Lapsurg of America. It received FDA 510(k) clearance on 1994-02-18 under 510(k) number K925499. 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 LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS?

LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-02-18. The listed applicant is Lapsurg of America. The 510(k) number is K925499.

When did LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1994-02-18, under 510(k) number K925499.

Who is the listed applicant for LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS?

The FDA 510(k) record lists Lapsurg of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS?

The FDA product code for LAPROSCOPIC/ENDOSCOPIC SURGICAL INSTRUMENTS is GCJ.

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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.

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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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