# D.Y. Instrument, Inc.

- Location (FDA's records): Cherry Hill, NJ
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: NRW (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 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
- Helio Medical Supplies, Inc.: 1 (https://510kreport.com/company/helio-medical-supplies)

## Recent decisions
- K040580: AIS100 Automatic Intramuscular Stimulator (Aug 26, 2004)

Source page: https://510kreport.com/company/dy-instrument