Laurus Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: CURVILINEAR SUTURE PLACEMENT SYSTEM, STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM, LAURUS NEEDLE CORE BIOPSY SYSTEM
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Laurus Medical Corp. Gastroenterology & Urology ✕
2 devices