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FDA 510(k)

REJUVENESS

K-Number: K974380 · 1998-04-03

ApplicantRejuveness Pharamceuticals, Inc.
Decision Date1998-04-03
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REJUVENESS is the device name listed in this FDA 510(k) record. The listed applicant is Rejuveness Pharamceuticals, Inc.. It received FDA 510(k) clearance on 1998-04-03 under 510(k) number K974380. The device is classified under product code MDA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REJUVENESS?

REJUVENESS is a medical device that received FDA 510(k) clearance on 1998-04-03. The listed applicant is Rejuveness Pharamceuticals, Inc.. The 510(k) number is K974380.

When did REJUVENESS receive FDA 510(k) clearance?

REJUVENESS received FDA 510(k) clearance on 1998-04-03, under 510(k) number K974380.

Who is the listed applicant for REJUVENESS?

The FDA 510(k) record lists Rejuveness Pharamceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REJUVENESS?

The FDA product code for REJUVENESS is MDA.

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Related Devices (Code: MDA)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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