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.
Clearance details
- Applicant
- Biowave Corporation
- Product code
- Code LIH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Attleboro, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.