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FDA 510(k)

LAPAROCISION SCOPE CONTROLLER SYSTEM

K-Number: K050027 · 2005-01-27

ApplicantGmp/Companies, Inc.
Decision Date2005-01-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROCISION SCOPE CONTROLLER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Gmp/Companies, Inc.. It received FDA 510(k) clearance on 2005-01-27 under 510(k) number K050027. 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 LAPAROCISION SCOPE CONTROLLER SYSTEM?

LAPAROCISION SCOPE CONTROLLER SYSTEM is a medical device that received FDA 510(k) clearance on 2005-01-27. The listed applicant is Gmp/Companies, Inc.. The 510(k) number is K050027.

When did LAPAROCISION SCOPE CONTROLLER SYSTEM receive FDA 510(k) clearance?

LAPAROCISION SCOPE CONTROLLER SYSTEM received FDA 510(k) clearance on 2005-01-27, under 510(k) number K050027.

Who is the listed applicant for LAPAROCISION SCOPE CONTROLLER SYSTEM?

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

What is the FDA product code for LAPAROCISION SCOPE CONTROLLER SYSTEM?

The FDA product code for LAPAROCISION SCOPE CONTROLLER SYSTEM 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.

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Other records listing Gmp/Companies, 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.

K030795LIFESYNE SYSTEMS

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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