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. Device class: Unclassified.
Clearance details
- Applicant
- Medevice Corporation
- Product code
- Code BWK
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pompano Beach, FL, US
Recent devices under product code BWK
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