ZIIP+ Device— 510(k) K212342
Substantially EquivalentZiip, Inc.
FDA 510(k) clearance K212342 for ZIIP+ Device, Substantially Equivalent on 2021-09-23. Applicant: Ziip, Inc.. Device class: 2.
Clearance details
- Applicant
- Ziip, Inc.
- 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
- Oakland, CA, US
Recent devices under product code NFO
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