Medical Device Recalls
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1 result found
510(K) Number: K020967 |
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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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TERUMO KHURI MYOCARDIAL PH MONITORING SYSTEM, CATALOG NUMBER 7205 | 2 | 09/29/2006 | Terumo Cardiovascular Systems Corp |
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