Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K911732 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopi... | 2 | 08/03/2005 | Argon Medical Devices, Inc |
| Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopi... | 2 | 08/03/2005 | Argon Medical Devices, Inc |
| Labeling is as follows: Product Labeling: ''***Argon Medical Devices***CUSTOM MANIFOLD KIT***R... | 2 | 08/03/2005 | Argon Medical Devices, Inc |
-







