Intravent Medical Partners, LP
United StatesFDA applicant, unverified
- Devices
- 5
What Intravent Medical Partners, LP makes
Intravent Medical Partners, LP manufactures the SOLOPASS System, a Class II medical device.
The SOLOPASS System is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
SOLOPASS 2.0 System Ref K251317
Regimes: 510(k) Registry: 510(k)SOLOPASS System Ref K203251
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intravent Medical Partners, LP have in the registry?
The registry currently lists 5 devices for Intravent Medical Partners, LP. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intravent Medical Partners, LP's devices?
Among its 5 most recently registered devices, Intravent Medical Partners, LP has devices listed in FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Intravent Medical Partners, LP's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Intravent Medical Partners, LP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intravent Medical Partners, LP in the registry?
The most recently registered devices listed for Intravent Medical Partners, LP include SOLOPASS 2.0 Patient Interface Device 1, SOLOPASS 2.0 Ultrasound Cable Assembly 1, SOLOPASS 2.0 Workstation 1 and SOLOPASS 2.0 System.