AHIP INTERNAL TRIGGER POINT WAND MODEL: 1— 510(k) DEN100023

Name: FDA 510(k) clearance DEN100023
Creator: U.S. Food and Drug Administration
Published: 2012-11-20

Unknown

National Center For Pelvic Pain Research Devices,

FDA 510(k) clearance DEN100023 for AHIP INTERNAL TRIGGER POINT WAND MODEL: 1, Unknown on 2012-11-20. Applicant: National Center For Pelvic Pain Research Devices,. Device class: 2.

Clearance details

Applicant: National Center For Pelvic Pain Research Devices,
Product code: Code OSD
Device class: Class 2
Regulation: 21 CFR 890.5670
Advisory panel: Physical Medicine
Date received: 2010-08-20
Decision date: 2012-11-20
Decision: Unknown
Clearance type: Post-NSE
Location: Sebastopol, CA, US

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