Cryocath Technologies, Inc.
Cryocath Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2008.
Top product codes for Cryocath Technologies, Inc.
Recent clearances by Cryocath Technologies, Inc.
- K081049 — FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12
- K070357 — FLEXCATH STEERABLE SHEATH & DILATOR
- K062140 — SURGIFROST XL CRYOSURGICAL DEVICE, MODEL 60SFXL; CRYOSURGICAL CONSOLE, MODEL 65CS1
- K053436 — SURGIFROST 6CM, 7CM AND 10 CM CRYOSURGICAL DEVICES PLUS FROSTBYTE CLAMP AND CRYOSURGICAL CONSOLE
- K040690 — SURGIFROST 10 CM CRYOSURGICAL DEVICE PLUS FROSTBYTE CLAMP AND CRYOSURGICAL CONSOLE
- K030303 — FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE AND CCT.2 CARDIAC CARDIAC CRYOABLATION CRYOCONSOLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.