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FDA 510(k)

SABRE MULTI-USE TROCAR SYSTEM

K-Number: K952977 · 1995-07-17

ApplicantEndoscopic Concepts, Inc.
Decision Date1995-07-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SABRE MULTI-USE TROCAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopic Concepts, Inc.. It received FDA 510(k) clearance on 1995-07-17 under 510(k) number K952977. 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 SABRE MULTI-USE TROCAR SYSTEM?

SABRE MULTI-USE TROCAR SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-17. The listed applicant is Endoscopic Concepts, Inc.. The 510(k) number is K952977.

When did SABRE MULTI-USE TROCAR SYSTEM receive FDA 510(k) clearance?

SABRE MULTI-USE TROCAR SYSTEM received FDA 510(k) clearance on 1995-07-17, under 510(k) number K952977.

Who is the listed applicant for SABRE MULTI-USE TROCAR SYSTEM?

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

What is the FDA product code for SABRE MULTI-USE TROCAR SYSTEM?

The FDA product code for SABRE MULTI-USE TROCAR 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 Endoscopic Concepts, 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.

K980804SABRE BT BLUNT0TIP SURGICAL TROCARK950500BASIC REUSABLE TROCAR SYSTEMK943976SABRE ULTIMATE SHIELDED TROCAR

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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