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FDA 510(k)

HYS-SURGIFLATOR 150P

K-Number: K983889 · 1999-01-14

ApplicantW.O.M. World of Medicine GmbH
Decision Date1999-01-14
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HYS-SURGIFLATOR 150P 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 1999-01-14 under 510(k) number K983889. 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 150P?

HYS-SURGIFLATOR 150P is a medical device that received FDA 510(k) clearance on 1999-01-14. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K983889.

When did HYS-SURGIFLATOR 150P receive FDA 510(k) clearance?

HYS-SURGIFLATOR 150P received FDA 510(k) clearance on 1999-01-14, under 510(k) number K983889.

Who is the listed applicant for HYS-SURGIFLATOR 150P?

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 150P?

The FDA product code for HYS-SURGIFLATOR 150P is HIG.

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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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