DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM— 510(k) K024307

Name: FDA 510(k) clearance K024307
Creator: U.S. Food and Drug Administration
Published: 2003-07-02

Substantially Equivalent

Sybaritic, Inc.

FDA 510(k) clearance K024307 for DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM, Substantially Equivalent on 2003-07-02. Applicant: Sybaritic, Inc.. Device class: 2.

Clearance details

Applicant: Sybaritic, Inc.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 2002-12-24
Decision date: 2003-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bloomington, MN, US

Download summary PDF View on FDA.gov ↗

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