Circulator Boot Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Circulator Boot Corp. makes
Circulator Boot Corp. manufactures medical-grade circulatory assist devices, including the Circulator Boot and Circulator Miniboot, designed to support peripheral blood flow in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
The Circulator Boot Ref K971026
Regimes: 510(k) Registry: 510(k)The Circulator Boot Ref K792354
Regimes: 510(k) Registry: 510(k)Circulator Boot Ref K082134
Regimes: 510(k) Registry: 510(k)Circulator Miniboot Ref K833627
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Circulator Boot Corp. have in the registry?
The registry currently lists 4 devices for Circulator Boot Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Circulator Boot Corp.'s devices?
Among its 4 most recently registered devices, Circulator Boot Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Circulator Boot Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Circulator Boot Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Circulator Boot Corp. in the registry?
The most recently registered devices listed for Circulator Boot Corp. include THE CIRCULATOR BOOT, CIRCULATOR BOOT and CIRCULATOR MINIBOOT.