# Oricare, Inc.

- Location (FDA's records): Quakertow., PA
- FDA decisions: 4 (2012–2014): 4 510(k) clearances
- Product codes: CBK (1), BTI (1), BSZ (1), FSY (1)
- Predicates its devices cite: 5 (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
- Datex-Ohmeda, Inc.: 1 (https://510kreport.com/company/datex-ohmeda)
- Datascope Corp., Patient Monitoring Division: 1 (https://510kreport.com/company/datascope-patient-monitoring-division)
- Draeger Medical, Inc.: 1 (https://510kreport.com/company/draeger-medical)
- Maquet GmbH: 1 (https://510kreport.com/company/maquet)
- STERIS Corporation: 1 (https://510kreport.com/company/steris)

## Recent decisions
- K131790: A9800 Anesthesia Workstation (May 9, 2014)
- K120931: Critical Care Ventilator (Jun 6, 2013)
- K122875: Oricare L2700 (Dec 18, 2012)
- K113338: Medical Air Compressor (Aug 10, 2012)

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