Cryocor, Inc. is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cryocor, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12, MODEL 3100 SERIES SHEATH INTRODUCER KITS, MODELS 3110, 3130
2
Total
2
Cleared
0
Denied
Cryocor, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cryocor, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cryocor, Inc.
2 devices