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FDA 510(k)

SURGIMAT

K-Number: K926259 · 1994-09-14

ApplicantW.O.M. World of Medicine GmbH
Decision Date1994-09-14
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SURGIMAT 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 1994-09-14 under 510(k) number K926259. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGIMAT?

SURGIMAT is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K926259.

When did SURGIMAT receive FDA 510(k) clearance?

SURGIMAT received FDA 510(k) clearance on 1994-09-14, under 510(k) number K926259.

Who is the listed applicant for SURGIMAT?

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 SURGIMAT?

The FDA product code for SURGIMAT is HET.

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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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