Karmel Medical Acoustic Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Karmel Medical Acoustic Technologies, Ltd. makes
Karmel Medical Acoustic Technologies, Ltd. manufactures the Pulmotrack Model 1010, a device designed for respiratory monitoring and tracking lung function parameters in clinical settings.
The Pulmotrack Model 1010 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pulmotrack, Model 1010 Ref K980878
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Karmel Medical Acoustic Technologies, Ltd. have in the registry?
The registry currently lists 1 device for Karmel Medical Acoustic Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Karmel Medical Acoustic Technologies, Ltd.'s devices?
Among its 1 most recently registered device, Karmel Medical Acoustic Technologies, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Karmel Medical Acoustic Technologies, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Karmel Medical Acoustic Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Karmel Medical Acoustic Technologies, Ltd. in the registry?
The most recently registered devices listed for Karmel Medical Acoustic Technologies, Ltd. include PULMOTRACK, MODEL 1010.