Strom Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Strom Corp. makes
Strom Corp. manufactures mechanical ventilator assist devices, including the PNEUMO PULSSOR III, PNEUMOPULSSOR (PPS II), and PNEUMO PULSSOR. These devices are designed to provide intermittent positive pressure ventilation support for patients, aiding respiration during medical procedures or recovery.
The company’s products fall under FDA Class II regulation and are listed via the 510(k) pathway. Strom Corp. is based in the United States.
Catalogue
Pneumo Pulssor Iii Ref K821570
Regimes: 510(k) Registry: 510(k)Pneumopulssor (Pps Ii) Ref K821265
Regimes: 510(k) Registry: 510(k)Pneumo Pulssor Ref K813438
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Strom Corp. have in the registry?
The registry currently lists 3 devices for Strom Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Strom Corp.'s devices?
Among its 3 most recently registered devices, Strom Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Strom Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Strom Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Strom Corp. in the registry?
The most recently registered devices listed for Strom Corp. include PNEUMO PULSSOR III, PNEUMOPULSSOR (PPS II) and PNEUMO PULSSOR.