Johnson & Johnson Professionals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SIPHONGUARD CSF CONTROL DEVICE, CODMAN ETHISORB DURA PATCH, CODMAN MICROSENSOR VENTRICULAR CATHETER KIT
206
Total
184
Cleared
0
Denied
FDA 510(k) Regulatory Record - Johnson & Johnson Professionals, Inc. Physical Medicine ✕
3 devices