BRAINPORT V100 DEVICE— 510(k) DEN130039
UnknownWicab, Inc.
FDA 510(k) clearance DEN130039 for BRAINPORT V100 DEVICE, Unknown on 2015-06-18. Applicant: Wicab, Inc.. Device class: 2.
Clearance details
- Applicant
- Wicab, Inc.
- Product code
- Code PIC
- Device class
- Class 2
- Regulation
- 21 CFR 886.5905
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Philedelphia, PA, US
Recent devices under product code PIC
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