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FDA 510(k)

HYS-SURGIFLATOR VP

K-Number: K933847 · 1995-08-15

ApplicantW.O.M. World of Medicine GmbH
Decision Date1995-08-15
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HYS-SURGIFLATOR VP 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 1995-08-15 under 510(k) number K933847. 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 VP?

HYS-SURGIFLATOR VP is a medical device that received FDA 510(k) clearance on 1995-08-15. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K933847.

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

HYS-SURGIFLATOR VP received FDA 510(k) clearance on 1995-08-15, under 510(k) number K933847.

Who is the listed applicant for HYS-SURGIFLATOR VP?

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 VP?

The FDA product code for HYS-SURGIFLATOR VP 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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