REJUVENESS— 510(k) K974380

Substantially Equivalent

Rejuveness Pharamceuticals, Inc.

FDA 510(k) clearance K974380 for REJUVENESS, Substantially Equivalent on 1998-04-03. Applicant: Rejuveness Pharamceuticals, Inc.. Device class: 1.

Clearance details

Applicant: Rejuveness Pharamceuticals, Inc.
Product code: Code MDA
Device class: Class 1
Regulation: 21 CFR 878.4025
Advisory panel: General, Plastic Surgery
Date received: 1997-10-21
Decision date: 1998-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ballston Spa, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.