Kontron Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATIONS TO INTRA-AORTIC BALLOONS, MODIFICATION OF INTRA-AORTIC BALLOON CATHETERS, INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATION
57
Total
57
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kontron Instruments, Inc. General Hospital ✕
1 devices