Interspec, Inc.
United StatesFDA applicant, unverified
- Devices
- 17
What Interspec, Inc. makes
Interspec, Inc. manufactures ultrasound imaging systems and Doppler flowmeters, including standalone units and modified versions for specialized applications. Their portfolio includes transcranial pulsed wave Doppler devices, such as the 2 MHz model, and systems like the Cardioscan with Doppler capabilities. The InterSpec Apogee series encompasses ultrasound imaging systems with Doppler flowmeter functionality, including variations like the RX400 model. Neurological monitoring devices, such as NeuroTrac, are also part of their offerings.
These devices are classified under Class II by the FDA and are subject to 510(k) clearance requirements. The company’s products are listed in the FDA’s 510(k) registry. Interspec, Inc. is based in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Interspec, Inc. have in the registry?
The registry currently lists 17 devices for Interspec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interspec, Inc.'s devices?
Among its 17 most recently registered devices, Interspec, Inc. has devices listed in FDA 510(k) (17 devices).
What risk classes do Interspec, Inc.'s devices fall under?
Among its 17 most recently registered devices, the classes recorded for Interspec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interspec, Inc. in the registry?
The most recently registered devices listed for Interspec, Inc. include CARDIOSCAN WITH DOPPLER OPTION, INTERSPEC APOGEE, ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETER and ULTRASONIC IMAGING SYSTEM (MODIFIED).