REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S— 510(k) K050046

Substantially Equivalent

Compex Technologies, Inc.

FDA 510(k) clearance K050046 for REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S, Substantially Equivalent on 2005-04-13. Applicant: Compex Technologies, Inc..

Clearance details

Applicant: Compex Technologies, Inc.
Product code: Code IPF
Advisory panel: Physical Medicine
Date received: 2005-01-10
Decision date: 2005-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Brighton, MN, US

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