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FDA 510(k)

SURGIMOTOR

K-Number: K954470 · 1995-12-08

ApplicantW.O.M. World of Medicine GmbH
Decision Date1995-12-08
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGIMOTOR is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 1995-12-08 under 510(k) number K954470. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGIMOTOR?

SURGIMOTOR is a medical device that received FDA 510(k) clearance on 1995-12-08. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K954470.

When did SURGIMOTOR receive FDA 510(k) clearance?

SURGIMOTOR received FDA 510(k) clearance on 1995-12-08, under 510(k) number K954470.

Who is the listed applicant for SURGIMOTOR?

The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGIMOTOR?

The FDA product code for SURGIMOTOR is GEY.

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Other records listing W.O.M. World of Medicine GmbH 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.

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Related Devices (Code: GEY)

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

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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