Medical Device Recalls
-
1 result found
510(K) Number: K792159 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODOC - Product Usage: intended to convert elec... | 2 | 10/21/2020 | Bien-Air Surgery Sa |
-