Versaflex Delivery Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Versaflex Delivery Systems, Inc. makes
Versaflex Delivery Systems, Inc. manufactures the VERSAFLEX DELTA ST MONITOR, a device used for intravascular monitoring, and the BUCHBINDER MULTIFLEX GUIDEWIRE, a guidewire designed for coronary and peripheral vascular procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Versaflex(Tm) Delta St(Tm) Monitor Ref K863922
Regimes: 510(k) Registry: 510(k)Buchbinder(Tm) Multiflex(Tm) Guidewire Ref K862937
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Versaflex Delivery Systems, Inc. have in the registry?
The registry currently lists 2 devices for Versaflex Delivery Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Versaflex Delivery Systems, Inc.'s devices?
Among its 2 most recently registered devices, Versaflex Delivery Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Versaflex Delivery Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Versaflex Delivery Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Versaflex Delivery Systems, Inc. in the registry?
The most recently registered devices listed for Versaflex Delivery Systems, Inc. include VERSAFLEX(TM) DELTA ST(TM) MONITOR and BUCHBINDER(TM) MULTIFLEX(TM) GUIDEWIRE.