Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K925079 |
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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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ENDOPLUS; Precision Laparoscopic Instruments; REF 345VA; Description 5 mm Traumatic Grasper S/A, S... | 2 | 09/21/2013 | Endoplus, Inc. |
ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description 5mm Atraumatic Grasper S/A, S... | 2 | 09/21/2013 | Endoplus, Inc. |
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