# Itamar Medical (C.M.) 1997, Ltd.

- Location (FDA's records): Hasbrouck Heights, NJ
- FDA decisions: 3 (2001–2002): 3 510(k) clearances
- Product codes: MNR (2), DQK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Itamar Medical, Ltd.: 1 (https://510kreport.com/company/itamar-medical)

## Its most-cited devices
- K001852: Peripheral Arterial Tonometer-Pat 1000RD Device (2001), cited by 1

## Recent decisions
- K010156: Sleep Pat 200 Device (Jun 19, 2002)
- K010739: Watch-Pat 100 (Nov 6, 2001)
- K001852: Peripheral Arterial Tonometer-Pat 1000RD Device (Feb 21, 2001)

Source page: https://510kreport.com/company/itamar-medical-cm-1997