PINOOK STIMULATOR— 510(k) K132563
Substantially EquivalentPinook USA
FDA 510(k) clearance K132563 for PINOOK STIMULATOR, Substantially Equivalent on 2014-04-24. Applicant: Pinook USA.
Clearance details
- Applicant
- Pinook USA
- Product code
- Code NUH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.