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FDA 510(k)

ARGUS LAPAROSCOPY INSTRUMENT SYSTEM

K-Number: K950378 · 1995-02-09

ApplicantArgus Medical Co., Inc.
Decision Date1995-02-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGUS LAPAROSCOPY INSTRUMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Argus Medical Co., Inc.. It received FDA 510(k) clearance on 1995-02-09 under 510(k) number K950378. 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 ARGUS LAPAROSCOPY INSTRUMENT SYSTEM?

ARGUS LAPAROSCOPY INSTRUMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1995-02-09. The listed applicant is Argus Medical Co., Inc.. The 510(k) number is K950378.

When did ARGUS LAPAROSCOPY INSTRUMENT SYSTEM receive FDA 510(k) clearance?

ARGUS LAPAROSCOPY INSTRUMENT SYSTEM received FDA 510(k) clearance on 1995-02-09, under 510(k) number K950378.

Who is the listed applicant for ARGUS LAPAROSCOPY INSTRUMENT SYSTEM?

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

What is the FDA product code for ARGUS LAPAROSCOPY INSTRUMENT SYSTEM?

The FDA product code for ARGUS LAPAROSCOPY INSTRUMENT SYSTEM is GCJ.

Related Clinical Trials

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Other records listing Argus Medical Co., 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.

K950255ARGUS HYSTEROSCOPY INSTRUMENT SYSTEMK951624ARGUS MEDICAL COMPANY LAPAROSCOPIC DISCECTOMY INSTRUMENT SYSTEMK950242ARGUS ARTHROSCOPY INSTRUMENT SYSTEMK950297ARGUS ENDOSCOPIC PLASTIC SURGERY INSTRUMENT SYSTEMK946011ARGUS SINUS ENDOSCOPY INSTRUMENT SYSTEM

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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