510(k) K202913
K202913 is an FDA 510(k) premarket notification submitted by Memory MD, Inc. for the device "NeuroCap (Model DEC22)". The FDA issued a decision of Substantially Equivalent on Mar 5, 2021. The device falls under product code GXY (Electrode, Cutaneous), a Class II device regulated under 21 CFR 882.1320. Memory MD, Inc. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 5, 2021
- Date Received
- Sep 29, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Cutaneous
- Device Class
- Class II
- Regulation Number
- 882.1320
- Review Panel
- NE
- Submission Type
- 510(k)