reSet— 510(k) DEN160018
UnknownPear Therapeutics, Inc.
FDA 510(k) clearance DEN160018 for reSet, Unknown on 2017-09-14. Applicant: Pear Therapeutics, Inc.. Device class: 2.
Clearance details
- Applicant
- Pear Therapeutics, Inc.
- Product code
- Code PWE
- Device class
- Class 2
- Regulation
- 21 CFR 882.5801
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Boston, MA, US
Recent devices under product code PWE
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