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FDA 510(k)

MEDUS GMBH

K-Number: K853153 · 1985-08-07

ApplicantCorkes Medical Co.
Decision Date1985-08-07
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDUS GMBH is the device name listed in this FDA 510(k) record. The listed applicant is Corkes Medical Co.. It received FDA 510(k) clearance on 1985-08-07 under 510(k) number K853153. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDUS GMBH?

MEDUS GMBH is a medical device that received FDA 510(k) clearance on 1985-08-07. The listed applicant is Corkes Medical Co.. The 510(k) number is K853153.

When did MEDUS GMBH receive FDA 510(k) clearance?

MEDUS GMBH received FDA 510(k) clearance on 1985-08-07, under 510(k) number K853153.

Who is the listed applicant for MEDUS GMBH?

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

What is the FDA product code for MEDUS GMBH?

The FDA product code for MEDUS GMBH is GEN.

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Related Devices (Code: GEN)

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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