REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S— 510(k) K050046
Substantially EquivalentCompex 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.. Device class: 2.
Clearance details
- Applicant
- Compex Technologies, Inc.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Brighton, MN, US
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