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FDA 510(k)

TROCARS

K-Number: K922685 · 1993-04-05

ApplicantEndoscopic Technologies, Inc.
Decision Date1993-04-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TROCARS is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopic Technologies, Inc.. It received FDA 510(k) clearance on 1993-04-05 under 510(k) number K922685. 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 TROCARS?

TROCARS is a medical device that received FDA 510(k) clearance on 1993-04-05. The listed applicant is Endoscopic Technologies, Inc.. The 510(k) number is K922685.

When did TROCARS receive FDA 510(k) clearance?

TROCARS received FDA 510(k) clearance on 1993-04-05, under 510(k) number K922685.

Who is the listed applicant for TROCARS?

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

What is the FDA product code for TROCARS?

The FDA product code for TROCARS is GCJ.

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Other records listing Endoscopic 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.

K060101ESTECH AORTIC EASY FLOW CANNULAK053326ESTECH COBRA ELECTROSURGICAL UNIT & CABLEK053100ESTECH COBRA BIPOLAR SYSTEMK946105ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIESK945978TUBING, NONINVASIVEK945979TROCAR/CANNULA

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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.

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

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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