NeuroCap— 510(k) K172866
Substantially EquivalentMemory MD, Inc.
FDA 510(k) clearance K172866 for NeuroCap, Substantially Equivalent on 2018-04-27. Applicant: Memory MD, Inc.. Device class: 2.
Clearance details
- Applicant
- Memory MD, Inc.
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
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More clearances from Memory MD, Inc.
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