Integra Neurocare, LLC - FDA 510(k) Cleared Devices
Recent clearances: NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33, BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730), MAURICE WORLDWIDE SHUNT SYSTEM
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Integra Neurocare, LLC Cardiovascular ✕
1 devices