Nautilus BrainPulse 1000— 510(k) DEN140040
UnknownJan Medical, Inc.
FDA 510(k) clearance DEN140040 for Nautilus BrainPulse 1000, Unknown on 2016-08-01. Applicant: Jan Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Jan Medical, Inc.
- Product code
- Code POP
- Device class
- Class 2
- Regulation
- 21 CFR 882.1630
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Mountain View, CA, US
Recent devices under product code POP
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