Endocision Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Endocision Technologies, Inc. makes
Endocision Technologies, Inc. manufactures the Celsio Flexible Cryocatheter System, a device used for cryoablation procedures to treat cardiac arrhythmias by freezing tissue.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The product is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Celsio Flexible Cryocatheter System Ref K240776
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endocision Technologies, Inc. have in the registry?
The registry currently lists 1 device for Endocision Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endocision Technologies, Inc.'s devices?
Among its 1 most recently registered device, Endocision Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Endocision Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endocision Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endocision Technologies, Inc. in the registry?
The most recently registered devices listed for Endocision Technologies, Inc. include Celsio Flexible Cryocatheter System.