Jms North America Corp. - FDA 510(k) Cleared Devices
Recent clearances: JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300, A.V. FISTULA BLUNT NEEDLE SET, JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Jms North America Corp. Cardiovascular ✕
1 devices