N.P.N.T., Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What N.P.N.T., Inc. makes
N.P.N.T., Inc. manufactures the Heart Protector (Ver. 1996), a medical device designed for cardiac protection during specific procedures or conditions. This product is intended to mitigate risks associated with heart-related interventions, though its exact clinical application is tied to the 1996 iteration of the device.
The Heart Protector (Ver. 1996) is classified as a Class II device under FDA regulations and has been submitted for clearance via the 510(k) pathway. The company is based in the United States, where its device portfolio is tracked in relevant regulatory registries.
Catalogue
Heart Protector (Ver 1996) Ref K965158
510(k) 510(k)
Frequently asked questions
How many devices does N.P.N.T., Inc. have in the registry?
The registry currently lists 1 device for N.P.N.T., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list N.P.N.T., Inc.'s devices?
Among its 1 most recently registered device, N.P.N.T., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do N.P.N.T., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for N.P.N.T., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from N.P.N.T., Inc. in the registry?
The most recently registered devices listed for N.P.N.T., Inc. include HEART PROTECTOR (VER 1996).