allay Nerve Cap— 510(k) DEN230061
UnknownTulavi Therapeutics
FDA 510(k) clearance DEN230061 for allay Nerve Cap, Unknown on 2024-07-16. Applicant: Tulavi Therapeutics. Device class: 2.
Clearance details
- Applicant
- Tulavi Therapeutics
- Product code
- Code SBG
- Device class
- Class 2
- Regulation
- 21 CFR 882.5260
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Lost Gatos, CA, US
Recent devices under product code SBG
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