Medical Device Recalls
-
|
1 result found
510(K) Number: K940261 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products | 2 | 07/12/2014 |
FEI # 2246821 MTI Precision Products LLC. |
-







