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FDA 510(k)

HYDROGUM

K-Number: K974704 · 1998-01-29

Decision Date1998-01-29
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYDROGUM is the device name listed in this FDA 510(k) record. The listed applicant is Zhermack S.P.A.. It received FDA 510(k) clearance on 1998-01-29 under 510(k) number K974704. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROGUM?

HYDROGUM is a medical device that received FDA 510(k) clearance on 1998-01-29. The listed applicant is Zhermack S.P.A.. The 510(k) number is K974704.

When did HYDROGUM receive FDA 510(k) clearance?

HYDROGUM received FDA 510(k) clearance on 1998-01-29, under 510(k) number K974704.

Who is the listed applicant for HYDROGUM?

The FDA 510(k) record lists Zhermack S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDROGUM?

The FDA product code for HYDROGUM is ELW.

Related Clinical Trials

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.

Other records listing Zhermack S.P.A. 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.

View all 19 devices →

Related Devices (Code: ELW)

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.

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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