MUSCLE STIMULATION SYSTEM— 510(k) K123642
Substantially EquivalentNiveus Medical, Inc.
FDA 510(k) clearance K123642 for MUSCLE STIMULATION SYSTEM, Substantially Equivalent on 2013-03-29. Applicant: Niveus Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Niveus Medical, 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
- Hillsborough, CA, US
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