Medical Device Recalls
-
|
1 result found
510(K) Number: K003075 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Puritan Bennett KnightStar 330 Bi-Level Ventilator, Catalogue Numbers: Y-KS330-NA, Y-KS330-SD, DSY-K... | 2 | 01/09/2007 | Puritan Bennett Corporation |
-







