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FDA 510(k)

HYS-SURGIFLATOR

K-Number: K924523 · 1995-04-11

ApplicantW.O.M. World of Medicine GmbH
Decision Date1995-04-11
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HYS-SURGIFLATOR 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 1995-04-11 under 510(k) number K924523. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYS-SURGIFLATOR?

HYS-SURGIFLATOR is a medical device that received FDA 510(k) clearance on 1995-04-11. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K924523.

When did HYS-SURGIFLATOR receive FDA 510(k) clearance?

HYS-SURGIFLATOR received FDA 510(k) clearance on 1995-04-11, under 510(k) number K924523.

Who is the listed applicant for HYS-SURGIFLATOR?

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 HYS-SURGIFLATOR?

The FDA product code for HYS-SURGIFLATOR is HIG.

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

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Related Devices (Code: HIG)

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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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