RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL— 510(k) K020180
Substantially EquivalentWoodside Biomedical, Inc.
FDA 510(k) clearance K020180 for RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL, Substantially Equivalent on 2002-03-21. Applicant: Woodside Biomedical, Inc..
Clearance details
- Applicant
- Woodside Biomedical, Inc.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Forest, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.