ZIIP Device— 510(k) K161484
Substantially EquivalentZiip,Llc
FDA 510(k) clearance K161484 for ZIIP Device, Substantially Equivalent on 2017-02-24. Applicant: Ziip,Llc.
Clearance details
- Applicant
- Ziip,Llc
- Product code
- Code NFO
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Piedmont, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.