Medical Device Recalls
-
1 result found
510(K) Number: K162053 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
INVUITY(R) PhotonBlade(TM), REF PB1 | 2 | 07/28/2017 | Invuity, Inc. |
-