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FDA 510(k)

OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES

K-Number: K923055 · 1992-11-23

ApplicantNumed Technologies, Inc.
Decision Date1992-11-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES is the device name listed in this FDA 510(k) record. The listed applicant is Numed Technologies, Inc.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K923055. 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 OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES?

OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Numed Technologies, Inc.. The 510(k) number is K923055.

When did OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES receive FDA 510(k) clearance?

OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES received FDA 510(k) clearance on 1992-11-23, under 510(k) number K923055.

Who is the listed applicant for OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES?

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

What is the FDA product code for OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES?

The FDA product code for OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES is GCJ.

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Other records listing Numed 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.

K922248MALLAWANY ATRAUMATIC TISSUE FORCEPSK930571REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATINGK931501NUMED DISPOSABLE ATT. NUMED HANDLE LAP. INST.K923126MALLAWANY TISSUE GRASPING FORCEPS

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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