Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K071226 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Spectranetics Turbo-Booster Laser Guide Catheter, 8 Fr, REF 518-063, Sterile EO, Spectranetics Corpo... | 2 | 08/04/2011 | Spectranetics Corporation |
Spectranetics Turbo-Booster Laser Guide Catheter, 7 Fr, REF 518-043, Sterile EO, Spectranetics Corpo... | 2 | 08/04/2011 | Spectranetics Corporation |
-