DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE— 510(k) K052289
Substantially EquivalentBiowave Corporation
FDA 510(k) clearance K052289 for DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE, Substantially Equivalent on 2005-12-13. Applicant: Biowave Corporation. Device class: 2.
Clearance details
- Applicant
- Biowave Corporation
- Product code
- Code LIH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Attleboro, MA, US
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