FDA 510(k) Applications Submitted by CRYOCATH TECHNOLOGIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K040690 03/16/2004 SURGIFROST 10 CM CRYOSURGICAL DEVICE PLUS FROSTBYTE CLAMP AND CRYOSURGICAL CONSOLE CRYOCATH TECHNOLOGIES, INC.
K070357 02/07/2007 FLEXCATH STEERABLE SHEATH & DILATOR CRYOCATH TECHNOLOGIES, INC.
K081049 04/14/2008 FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12 CRYOCATH TECHNOLOGIES, INC.
K062140 07/27/2006 SURGIFROST XL CRYOSURGICAL DEVICE, MODEL 60SFXL; CRYOSURGICAL CONSOLE, MODEL 65CS1 CRYOCATH TECHNOLOGIES, INC.
K053436 12/09/2005 SURGIFROST 6CM, 7CM AND 10 CM CRYOSURGICAL DEVICES PLUS FROSTBYTE CLAMP AND CRYOSURGICAL CONSOLE CRYOCATH TECHNOLOGIES, INC.
K030303 01/29/2003 FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE AND CCT.2 CARDIAC CARDIAC CRYOABLATION CRYOCONSOLE CRYOCATH TECHNOLOGIES, INC.


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