ORTHO DX NEUROMUSCULAR STIMULATOR— 510(k) K971542
Substantially EquivalentRehabilicare, Inc.
FDA 510(k) clearance K971542 for ORTHO DX NEUROMUSCULAR STIMULATOR, Substantially Equivalent on 1997-08-14. Applicant: Rehabilicare, Inc.. Device class: 2.
Clearance details
- Applicant
- Rehabilicare, 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
Recent devices under product code IPF
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Data sourced from openFDA. This site is unofficial and independent of the FDA.