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FDA 510(k)

SPECIMEN RETRIEVAL BAG

K-Number: K962395 · 1996-07-05

ApplicantApplied Medical Resources
Decision Date1996-07-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SPECIMEN RETRIEVAL BAG is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 1996-07-05 under 510(k) number K962395. 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 SPECIMEN RETRIEVAL BAG?

SPECIMEN RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 1996-07-05. The listed applicant is Applied Medical Resources. The 510(k) number is K962395.

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

SPECIMEN RETRIEVAL BAG received FDA 510(k) clearance on 1996-07-05, under 510(k) number K962395.

Who is the listed applicant for SPECIMEN RETRIEVAL BAG?

The FDA 510(k) record lists Applied Medical Resources as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECIMEN RETRIEVAL BAG?

The FDA product code for SPECIMEN RETRIEVAL BAG is GCJ.

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Other records listing Applied Medical Resources 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.

K200021Applied Medical AnoscopeK162676Voyant Open Fusion DeviceK153017Voyant Fine FusionK153288Voyant Open Fusion DeviceK151480Epix Electrosurgical Probe with Smoke EvacuationK100959SPECIMEN RETRIEVAL SYSTEM

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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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