Cryocath Technologies, Inc. is one of 657 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cryocath Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12, FLEXCATH STEERABLE SHEATH & DILATOR, SURGIFROST XL CRYOSURGICAL DEVICE, MODEL 60SFXL
6
Total
6
Cleared
0
Denied
Cryocath Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Kirkland, CA.
Historical record: 6 cleared submissions from 2003 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cryocath Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cryocath Technologies, Inc.
6 devices
Cleared
Jun 27, 2008
FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12
Cardiovascular
74d
Cleared
Dec 28, 2007
FLEXCATH STEERABLE SHEATH & DILATOR
Cardiovascular
324d
Cleared
Aug 24, 2006
SURGIFROST XL CRYOSURGICAL DEVICE, MODEL 60SFXL
Cardiovascular
28d
Cleared
Jan 13, 2006
SURGIFROST 6CM, 7CM AND 10 CM CRYOSURGICAL DEVICES PLUS FROSTBYTE CLAMP AND...
Cardiovascular
35d
Cleared
Apr 29, 2004
SURGIFROST 10 CM CRYOSURGICAL DEVICE PLUS FROSTBYTE CLAMP AND CRYOSURGICAL...
Cardiovascular
44d
Cleared
Apr 29, 2003
FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE AND CCT.2 CARDIAC CARDIAC...
General & Plastic Surgery
90d