Medical Device Recalls
-
|
1 result found
510(K) Number: K852544 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Kendall Monoject Syringe with Hypodermic Needle, 3cc syringe with 27 ga A-Bevel Needle (3cc- 27x1-1/... | 2 | 10/21/2006 |
FEI # 1317749 Kendall a Division of Tyco Healthcare Group LP |
-







