Medical Device Recalls
-
|
1 result found
510(K) Number: K161704 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 | 2 | 07/29/2025 | Phasor Health, LLC |
-







