Medical Device Recalls
-
|
1 result found
510(K) Number: K120820 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Giraffe Blue Spot PT LiteTM Phototherapy System, Model Numbers M1224917, M1231533, M1225025, M122496... | 2 | 01/31/2020 | Lumitex Inc |
-







