SONOPREP ULTRASONIC SKIN PERMEATION SYSTEM AND TOPICAL ANESTHETIC KIT, MODEL D2000— 510(k) K040525

Name: FDA 510(k) clearance K040525
Creator: U.S. Food and Drug Administration
Published: 2004-08-17

Unknown

Sontra Medical, Inc.

FDA 510(k) clearance K040525 for SONOPREP ULTRASONIC SKIN PERMEATION SYSTEM AND TOPICAL ANESTHETIC KIT, MODEL D2000, Unknown on 2004-08-17. Applicant: Sontra Medical, Inc.. Device class: 2.

Clearance details

Applicant: Sontra Medical, Inc.
Product code: Code NRJ
Device class: Class 2
Regulation: 21 CFR 878.4410
Advisory panel: General, Plastic Surgery
Date received: 2004-03-01
Decision date: 2004-08-17
Decision: Unknown
Clearance type: Traditional
Location: Franklin, MA, US

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