Paramed Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Paramed Technology, Inc. makes
Paramed Technology, Inc. manufactures automated blood pressure monitors, including the Model 9350 and Cardivan series, designed for clinical and home use to measure systolic and diastolic pressure.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Paramed Model 9350 Blood Pressure Monitor (9350) Ref K890198
Regimes: 510(k) Registry: 510(k)Cardivan Blood Pressure Monitor Ref K830682
Regimes: 510(k) Registry: 510(k)Cardivan Blood Pressure Monitor Ref K792226
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paramed Technology, Inc. have in the registry?
The registry currently lists 3 devices for Paramed Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paramed Technology, Inc.'s devices?
Among its 3 most recently registered devices, Paramed Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Paramed Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Paramed Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Paramed Technology, Inc. in the registry?
The most recently registered devices listed for Paramed Technology, Inc. include PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350) and CARDIVAN BLOOD PRESSURE MONITOR.