Gould, Inc.
United StatesFDA applicant, unverified
- Devices
- 31
What Gould, Inc. makes
Gould, Inc. manufactures medical devices for cardiac monitoring and hemodynamic measurement, including ECG stress testing systems, thermodilution catheters, pressure monitoring catheters, and physiological pressure transducers. Their portfolio also includes disposable transducers, pressure tubing for adult and pediatric use, and flow-directed thermal dilution catheters, alongside related accessories and disposable components for critical care applications.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. These products are primarily listed in the FDA’s 510(k) database. Gould, Inc. is based in the United States.
Catalogue
Search and filter all 31 devicesFrequently asked questions
How many devices does Gould, Inc. have in the registry?
The registry currently lists 31 devices for Gould, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gould, Inc.'s devices?
Among its 31 most recently registered devices, Gould, Inc. has devices listed in FDA 510(k) (31 devices).
What risk classes do Gould, Inc.'s devices fall under?
Among its 31 most recently registered devices, the classes recorded for Gould, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gould, Inc. in the registry?
The most recently registered devices listed for Gould, Inc. include C/PES 9201, ECG STRESS TESTING SYS, THERMODILUTION CATHETER, CRITIFLO & CRITIFLO DOME and MODEL SP5800 #8 FRENCH INTRO. KIT.