VEINOPLUS NEUROMUSCULAR STIMULATOR— 510(k) K072252
Substantially EquivalentAd Rem Technology Sarl
FDA 510(k) clearance K072252 for VEINOPLUS NEUROMUSCULAR STIMULATOR, Substantially Equivalent on 2008-01-30. Applicant: Ad Rem Technology Sarl. Device class: 2.
Clearance details
- Applicant
- Ad Rem Technology Sarl
- 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
- Potomac, MD, US
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