Srs Medical
United Statesfrom the FDA registration address FDA FEI 3033428382
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
CT3000Pro Ref K212830
Regimes: 510(k) Registry: 510(k)The Spanner Temporary Prostatic Stent Ref P060010
Regimes: PMA Registry: PMA
Company details
- FDA FEI number
- 3033428382
- Address
- 321 Billerica Rd, Chelmsford, MA, 01824
Frequently asked questions
How many devices does Srs Medical have in the registry?
The registry currently lists 2 devices for Srs Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Srs Medical's devices?
Among its 2 most recently registered devices, Srs Medical has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Srs Medical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Srs Medical's devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Srs Medical in the registry?
The most recently registered devices listed for Srs Medical include CT3000Pro and THE SPANNER TEMPORARY PROSTATIC STENT.