Pulse Metric, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Pulse Metric, Inc. makes
Pulse Metric, Inc. manufactures blood pressure monitoring systems, including portable and pathway-based devices designed for continuous or intermittent arterial blood pressure measurement. These systems are intended for clinical and point-of-care use, supporting real-time monitoring of hemodynamic parameters.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Dynapulse 5000A (DP5000A) Ref K945111
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Dynapulse 200M Ref K904739
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulse Metric, Inc. have in the registry?
The registry currently lists 5 devices for Pulse Metric, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulse Metric, Inc.'s devices?
Among its 5 most recently registered devices, Pulse Metric, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Pulse Metric, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pulse Metric, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulse Metric, Inc. in the registry?
The most recently registered devices listed for Pulse Metric, Inc. include DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEM, DYNAPULSE 5000A (DP5000A), DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM and DYNAPULSE 200M.