Medical Device Recalls
-
|
1 result found
510(K) Number: K980466 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| PER-FIT Percutaneous Dilational Tracheostomy Kit with Specialty Tracheostomy Tube REF # 511080 | 2 | 07/20/2004 | Smiths Medical ASD, Inc. |
-







