Medical Device Recalls
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1 result found
510(K) Number: K103726 |
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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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Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R) Take-Apart Endoscopi... | 2 | 07/18/2012 | Integra Limited |
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