Medical Device Recalls
-
|
1 to 4 of 4 Results
510(K) Number: K904172 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at... | 2 | 03/03/2016 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
| 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at... | 2 | 03/03/2016 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
| (Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a prede... | 2 | 03/03/2016 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
| (Stryker) AccuPlace Round Level Needle Guide; Assists the user with inserting a needle at a predeter... | 2 | 03/03/2016 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
-







