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. Device class: 2.
Clearance details
- Applicant
- Ziip,Llc
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Piedmont, CA, US
Recent devices under product code NFO
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