E-PULSE— 510(k) K091875
Substantially EquivalentMedevice Corporation
FDA 510(k) clearance K091875 for E-PULSE, Substantially Equivalent on 2009-12-07. Applicant: Medevice Corporation.
Clearance details
- Applicant
- Medevice Corporation
- Product code
- Code BWK
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pompano Beach, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.