Cardio Systems, Inc.
Cardio Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2013.
Top product codes for Cardio Systems, Inc.
Recent clearances by Cardio Systems, Inc.
- K131092 — STEALTH 360 ORBITAL PAD SYSTEM
- K081944 — MODIFICATION TO DIAMONDBACK 360 DEGREE ORBITAL ATHERECTOMY SYSTEM
- K972022 — ZAK-2000
- K934689 — LOW AIR LOSS MATTRESS, MODIFICATION
- K921500 — CENTRI-SAFE(TM) VALVE
- K882177 — ADD-ON TO CRITICAL PATIENT CARE BED
- K852736 — BAYLOR RAPID AUTOTRANSFUSION SYSTEM
- K792151 — OXYGENATOR GAS LINE FILTER
- K792152 — CARDIOPLEGIA SOLUTION ADMIN. SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.