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