Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K964929 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Locking Tear-Away Sheath Introducer Product Line. ACCUGUIDE SINGLE LUMEN 4FR PICC P460K 5/; P56... | 2 | 08/03/2005 | B. Braun Medical, Inc. |
CA 125 Controls, list 9C22-10; Abbott Laboratories, Abbott Park, IL 60064 | 3 | 01/10/2004 | Abbott Laboratories HPD/ADD/GPRD |
-