Rescare, Ltd.
Country not established
- Devices
- 5
What Rescare, Ltd. makes
Rescare, Ltd. manufactures positive airway pressure (PAP) therapy devices, including nasal and nasal/mouth CPAP and VPAP systems designed for continuous or variable pressure support during sleep. Their portfolio includes portable and clinical-grade systems, as well as nasal masks for airway management in respiratory conditions.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are intended for use in the United States, where they comply with U.S. medical device standards.
Catalogue
Sullivan Iii Nasal Cpap System Ref K930656
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Sullivan Passover Humidifer Ref K950582
Regimes: 510(k) Registry: 510(k)Sullivan Nasal Vpap System Ref K931884
Regimes: 510(k) Registry: 510(k)Sullivan Nose & Mouth Mask System Ref K952475
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rescare, Ltd. have in the registry?
The registry currently lists 5 devices for Rescare, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rescare, Ltd.'s devices?
Among its 5 most recently registered devices, Rescare, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Rescare, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Rescare, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rescare, Ltd. in the registry?
The most recently registered devices listed for Rescare, Ltd. include SULLIVAN III NASAL CPAP SYSTEM, RES CARE AUTO SET CLINICAL, PORTABLE SYSTEM, PORTABLE 2 SYSTEM, SULLIVAN PASSOVER HUMIDIFER and SULLIVAN NASAL VPAP SYSTEM.