# Memory MD, Inc.

- Location (FDA's records): New York, NY
- FDA decisions: 3 (2018–2021): 3 510(k) clearances
- Product codes: GXY (2), GWQ (1)
- 510(k) review time since 2016: median 157 days, against 150 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Hydrodot, Inc.: 1 (https://510kreport.com/company/hydrodot)
- Brainmaster Technologies, Inc.: 1 (https://510kreport.com/company/brainmaster-technologies)
- Wavi Co.: 1 (https://510kreport.com/company/wavi)

## Its most-cited devices
- K172866: NeuroCap (2018), cited by 1

## Recent decisions
- K202913: NeuroCap (Model DEC22) (Mar 5, 2021)
- K172866: NeuroCap (Apr 27, 2018)
- K173460: NeuroEEG (Feb 16, 2018)

Source page: https://510kreport.com/company/memory-md