Sontek Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Sontek Corp. makes
Sontek Corp. manufactures vascular catheters, including infusion and angiographic catheters designed for diagnostic and interventional procedures, as well as peripheral transluminal angioplasty devices for treating narrowed or blocked arteries.
The company’s portfolio is regulated under FDA Class II devices and is listed in the 510(k) clearance registry. Sontek Corp. is based in the United States.
Catalogue
Sontek Infusion Catheter Ref K831562
Regimes: 510(k) Registry: 510(k)Sontek Angiographic Catheter Ref K810508
Regimes: 510(k) Registry: 510(k)Peripheral Transluminal Argioplasty Ref K832279
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sontek Corp. have in the registry?
The registry currently lists 3 devices for Sontek Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sontek Corp.'s devices?
Among its 3 most recently registered devices, Sontek Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sontek Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sontek Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sontek Corp. in the registry?
The most recently registered devices listed for Sontek Corp. include SONTEK INFUSION CATHETER, SONTEK ANGIOGRAPHIC CATHETER and PERIPHERAL TRANSLUMINAL ARGIOPLASTY.