PANTHEON ELECTROSTIMULATOR— 510(k) K133980
Substantially EquivalentPantheon Research
FDA 510(k) clearance K133980 for PANTHEON ELECTROSTIMULATOR, Substantially Equivalent on 2014-11-07. Applicant: Pantheon Research. Device class: Unclassified.
Clearance details
- Applicant
- Pantheon Research
- Product code
- Code BWK
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Recent devices under product code BWK
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