Gesco Intl., Inc. - FDA 510(k) Cleared Devices
Recent clearances: PER-Q-CATH MID-LINE, UMBILI-CATH, UMBILI-CATH-S
26
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Gesco Intl., Inc. Neurology ✕
1 devices