Intertherapy, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Intertherapy, Inc. makes
Intertherapy, Inc. manufactures intravascular imaging systems, including catheters and imaging devices designed for coronary and peripheral vascular assessment. Their portfolio includes linear translator catheters and modified intravascular imaging systems, primarily used for visualizing blood vessels during interventional procedures.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company’s products are listed in the FDA’s 510(k) database, reflecting their compliance with US medical device regulations.
Catalogue
Intravascular Imaging System Ref K895159
Regimes: 510(k) Registry: 510(k)Interpret(Tm) Catheter Linear Translator Ref K913763
Regimes: 510(k) Registry: 510(k)Intravascular Imaging System/Modified Ref K910281
Regimes: 510(k) Registry: 510(k)Interpret(Tm) Intravascular Imaging Catheter Ref K912600
Regimes: 510(k) Registry: 510(k)Intravascular Imaging Systems Ref K900305
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intertherapy, Inc. have in the registry?
The registry currently lists 5 devices for Intertherapy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intertherapy, Inc.'s devices?
Among its 5 most recently registered devices, Intertherapy, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Intertherapy, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Intertherapy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intertherapy, Inc. in the registry?
The most recently registered devices listed for Intertherapy, Inc. include INTRAVASCULAR IMAGING SYSTEM, INTERPRET(TM) CATHETER LINEAR TRANSLATOR, INTRAVASCULAR IMAGING SYSTEM/MODIFIED and INTERPRET(TM) INTRAVASCULAR IMAGING CATHETER.