# Intercure, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2000–2002): 2 510(k) clearances
- Product codes: HCC (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Deepwell Dtx, Inc.: 1 (https://510kreport.com/company/deepwell-dtx)
- Palo Alto Health Sciences, Inc.: 1 (https://510kreport.com/company/palo-alto-health-sciences)
- Polar Wrap, LLC: 1 (https://510kreport.com/company/polar-wrap)

## Its most-cited devices
- K020399: Resperate; Model RR-150 (2002), cited by 3
- K000405: Intercure LTD. Respi-Low (2000), cited by 1

## Recent decisions
- K020399: Resperate; Model RR-150 (Jul 2, 2002)
- K000405: Intercure LTD. Respi-Low (May 17, 2000)

Source page: https://510kreport.com/company/intercure