Dynatech/Nevada, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
Catalogue
Impulse 3000 Defibrillator Analyzer Ref K934254
510(k) 510(k)Medsim 300 Patient Simulator Ref K935817
510(k) 510(k)Model 215M Patient Simulator Ref K897074
510(k) 510(k)Model 404A I.V. Infusion Pump Analyzer Ref K897096
510(k) 510(k)Cufflink Non-Invasive Blood Pressure Analyzer Ref K942546
510(k) 510(k)Model ECG100 Simulator Ref K897029
510(k) 510(k)
Frequently asked questions
How many devices does Dynatech/Nevada, Inc. have in the registry?
The registry currently lists 6 devices for Dynatech/Nevada, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dynatech/Nevada, Inc.'s devices?
Among its 6 most recently registered devices, Dynatech/Nevada, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Dynatech/Nevada, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Dynatech/Nevada, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dynatech/Nevada, Inc. in the registry?
The most recently registered devices listed for Dynatech/Nevada, Inc. include IMPULSE 3000 DEFIBRILLATOR ANALYZER, MEDSIM 300 PATIENT SIMULATOR, MODEL 215M PATIENT SIMULATOR and MODEL 404A I.V. INFUSION PUMP ANALYZER.