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FDA 510(k)

VP-1000; MED CAM 100; VP-3000A; MED CAM 300

K-Number: K032544 · 2003-09-02

Decision Date2003-09-02
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VP-1000; MED CAM 100; VP-3000A; MED CAM 300 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 2003-09-02 under 510(k) number K032544. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VP-1000; MED CAM 100; VP-3000A; MED CAM 300?

VP-1000; MED CAM 100; VP-3000A; MED CAM 300 is a medical device that received FDA 510(k) clearance on 2003-09-02. The listed applicant is Mgb Endoskopische Gerate GmbH (Berlin). The 510(k) number is K032544.

When did VP-1000; MED CAM 100; VP-3000A; MED CAM 300 receive FDA 510(k) clearance?

VP-1000; MED CAM 100; VP-3000A; MED CAM 300 received FDA 510(k) clearance on 2003-09-02, under 510(k) number K032544.

Who is the listed applicant for VP-1000; MED CAM 100; VP-3000A; MED CAM 300?

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 VP-1000; MED CAM 100; VP-3000A; MED CAM 300?

The FDA product code for VP-1000; MED CAM 100; VP-3000A; MED CAM 300 is FET.

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: FET)

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

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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