MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-12-08 for manufactured by .
| Product Code | OAP |
| Date Received | 2016-12-08 |
| Device Availability | I |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |