Haemoband Surgical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SleeveLUX 24 Anoscope/Proctoscope (P2001), HAEMOBAND MULTI-LIGATOR
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Haemoband Surgical, Ltd. Gastroenterology & Urology ✕
2 devices