Medical Device Recalls
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1 result found
510(K) Number: K993531 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Passport 2/Passport 2 LT Vital Signs Monitor. Multi-parameter patient monitoring system. | 3 | 07/20/2004 |
FEI # 2221819 Datascope Corp |
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