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FDA 510(k)

MGB DISPOSABLE RETRIEVAL BAG LAPBAG

K-Number: K093194 · 2010-03-03

Decision Date2010-03-03
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MGB DISPOSABLE RETRIEVAL BAG LAPBAG is the device name listed in this FDA 510(k) record. The listed applicant is Mgb Endoskopische Gerate GmbH (Berlin). It received FDA 510(k) clearance on 2010-03-03 under 510(k) number K093194. 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 MGB DISPOSABLE RETRIEVAL BAG LAPBAG?

MGB DISPOSABLE RETRIEVAL BAG LAPBAG is a medical device that received FDA 510(k) clearance on 2010-03-03. The listed applicant is Mgb Endoskopische Gerate GmbH (Berlin). The 510(k) number is K093194.

When did MGB DISPOSABLE RETRIEVAL BAG LAPBAG receive FDA 510(k) clearance?

MGB DISPOSABLE RETRIEVAL BAG LAPBAG received FDA 510(k) clearance on 2010-03-03, under 510(k) number K093194.

Who is the listed applicant for MGB DISPOSABLE RETRIEVAL BAG LAPBAG?

The FDA 510(k) record lists Mgb Endoskopische Gerate GmbH (Berlin) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MGB DISPOSABLE RETRIEVAL BAG LAPBAG?

The FDA product code for MGB DISPOSABLE RETRIEVAL BAG LAPBAG 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.

Other records listing Mgb Endoskopische Gerate GmbH (Berlin) 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.

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.

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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