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FDA 510(k)

EAGLE ENDO SPECIMEN RETRIEVAL BAG

K-Number: K001264 · 2000-05-30

ApplicantEagle Endoscopic, Inc.
Decision Date2000-05-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EAGLE ENDO SPECIMEN RETRIEVAL BAG is the device name listed in this FDA 510(k) record. The listed applicant is Eagle Endoscopic, Inc.. It received FDA 510(k) clearance on 2000-05-30 under 510(k) number K001264. 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 EAGLE ENDO SPECIMEN RETRIEVAL BAG?

EAGLE ENDO SPECIMEN RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 2000-05-30. The listed applicant is Eagle Endoscopic, Inc.. The 510(k) number is K001264.

When did EAGLE ENDO SPECIMEN RETRIEVAL BAG receive FDA 510(k) clearance?

EAGLE ENDO SPECIMEN RETRIEVAL BAG received FDA 510(k) clearance on 2000-05-30, under 510(k) number K001264.

Who is the listed applicant for EAGLE ENDO SPECIMEN RETRIEVAL BAG?

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

What is the FDA product code for EAGLE ENDO SPECIMEN RETRIEVAL BAG?

The FDA product code for EAGLE ENDO SPECIMEN RETRIEVAL BAG 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 Eagle Endoscopic, 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.

K001994EEI SLUSH PAN DRAPE

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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