Curative Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
What Curative Medical, Inc. makes
Curative Medical, Inc. manufactures continuous positive airway pressure (CPAP) systems, including models with integrated heated humidifiers, as well as nasal masks designed for sleep therapy. The company also produces balloon dilatation catheters for percutaneous transluminal angioplasty (PTA) procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
K Series Cpap Systems Ref K131702
510(k) 510(k)K Series Cpap Systems Ref K123897
510(k) 510(k)K Series Cpap Systems Ref K130828
510(k) 510(k)K Series Cpap System With Heated Humidifer Ref K120285
510(k) 510(k)Navajo Pta Balloon Dilatation Catheter Ref K141354
510(k) 510(k)BESTFIT2 Nasal Mask Ref K130663
510(k) 510(k)
Frequently asked questions
How many devices does Curative Medical, Inc. have in the registry?
The registry currently lists 6 devices for Curative Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curative Medical, Inc.'s devices?
Among its 6 most recently registered devices, Curative Medical, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Curative Medical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Curative Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curative Medical, Inc. in the registry?
The most recently registered devices listed for Curative Medical, Inc. include K SERIES CPAP SYSTEMS, K SERIES CPAP SYSTEM WITH HEATED HUMIDIFER, NAVAJO PTA BALLOON DILATATION CATHETER and BESTFIT2 NASAL MASK.