Cryocor, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Cryocor, Inc. makes
Cryocor, Inc. manufactures cryoablation surgical probes, including the Model 1250 (Breva) series and associated accessories like the Model 1255-15-12 probe, designed for tissue freezing procedures. The company also produces sheath introducer kits, such as the Model 3100 series (including Models 3110 and 3130), used for guiding cryoprobes during surgical interventions.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Cryocor, Inc. have in the registry?
The registry currently lists 2 devices for Cryocor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryocor, Inc.'s devices?
Among its 2 most recently registered devices, Cryocor, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cryocor, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cryocor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryocor, Inc. in the registry?
The most recently registered devices listed for Cryocor, Inc. include CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 and MODEL 3100 SERIES SHEATH INTRODUCER KITS, MODELS 3110, 3130.