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FDA 510(k)

CONMED BEAMER SYSTEM C600

K-Number: K081678 · 2008-07-29

ApplicantKls Martin GmbH + Co. KG
Decision Date2008-07-29
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED BEAMER SYSTEM C600 is the device name listed in this FDA 510(k) record. The listed applicant is Kls Martin GmbH + Co. KG. It received FDA 510(k) clearance on 2008-07-29 under 510(k) number K081678. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED BEAMER SYSTEM C600?

CONMED BEAMER SYSTEM C600 is a medical device that received FDA 510(k) clearance on 2008-07-29. The listed applicant is Kls Martin GmbH + Co. KG. The 510(k) number is K081678.

When did CONMED BEAMER SYSTEM C600 receive FDA 510(k) clearance?

CONMED BEAMER SYSTEM C600 received FDA 510(k) clearance on 2008-07-29, under 510(k) number K081678.

Who is the listed applicant for CONMED BEAMER SYSTEM C600?

The FDA 510(k) record lists Kls Martin GmbH + Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONMED BEAMER SYSTEM C600?

The FDA product code for CONMED BEAMER SYSTEM C600 is GEI.

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Other records listing Kls Martin GmbH + Co. KG as applicant

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Related Devices (Code: GEI)

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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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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