Medical Device Recalls
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1 result found
510(K) Number: K030768 |
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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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Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 (List Number 06F12-09; Lot Number 0710... | 3 | 11/02/2012 | Abbott Point Of Care Inc. |
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