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FDA 510(k)

ENDOSCOPIC CLIP APPLIER

K-Number: K911817 · 1991-06-11

ApplicantSurgitech C/O Collier, Shannon, Rill & Scott
Decision Date1991-06-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Surgitech C/O Collier, Shannon, Rill & Scott. It received FDA 510(k) clearance on 1991-06-11 under 510(k) number K911817. 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 ENDOSCOPIC CLIP APPLIER?

ENDOSCOPIC CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1991-06-11. The listed applicant is Surgitech C/O Collier, Shannon, Rill & Scott. The 510(k) number is K911817.

When did ENDOSCOPIC CLIP APPLIER receive FDA 510(k) clearance?

ENDOSCOPIC CLIP APPLIER received FDA 510(k) clearance on 1991-06-11, under 510(k) number K911817.

Who is the listed applicant for ENDOSCOPIC CLIP APPLIER?

The FDA 510(k) record lists Surgitech C/O Collier, Shannon, Rill & Scott as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC CLIP APPLIER?

The FDA product code for ENDOSCOPIC CLIP APPLIER 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 Surgitech C/O Collier, Shannon, Rill & Scott 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.

K874450SCHACHNER-OVIL RAPITRAC PERCUTAN. TRACHEOSTOMY KIT

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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