Medical Device Recalls
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41 to 45 of 45 Results
510(K) Number: K915183 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Terumo Perfusion System 8000 Base, 4 pump, 220/240v; Model 8000; Catalog No. 16405. | 2 | 12/07/2006 | Terumo Cardiovascular Systems Corp |
Terumo Perfusion System 8000 Base, 5 pump, 115v; Model 8000; Catalog No. 16401. | 2 | 12/07/2006 | Terumo Cardiovascular Systems Corp |
Terumo Perfusion System 8000 Base, 4 pump, 100v, Model 8000; Catalog No. 16409. | 2 | 12/07/2006 | Terumo Cardiovascular Systems Corp |
Terumo Perfusion System 8000 Base, 5 pump, 100v, Model 8000; Catalog No. 16410. | 2 | 12/07/2006 | Terumo Cardiovascular Systems Corp |
Terumo Perfusion System 8000 Base, 5 pump, 220240v; Model 8000; Catalog No. 16406. | 2 | 12/07/2006 | Terumo Cardiovascular Systems Corp |
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