Seismed Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Seismocardiograph - Scg(Tm) 1000 Series Ref K892323
Regimes: 510(k) Registry: 510(k)Modified Seismocardiograph Ref K900130
Regimes: 510(k) Registry: 510(k)Modified Seismocardiograph Ref K910994
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seismed Instruments, Inc. have in the registry?
The registry currently lists 3 devices for Seismed Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seismed Instruments, Inc.'s devices?
Among its 3 most recently registered devices, Seismed Instruments, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Seismed Instruments, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Seismed Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seismed Instruments, Inc. in the registry?
The most recently registered devices listed for Seismed Instruments, Inc. include SEISMOCARDIOGRAPH - SCG(TM) 1000 SERIES and MODIFIED SEISMOCARDIOGRAPH.