Medical Device Recalls
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1 result found
510(K) Number: K973896 |
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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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Datex-Ohmeda Aestiva/5 Active Gas Scavenging System used with a Model 7900 Ventillator, on a Aestiva... | 2 | 07/20/2004 | Datex-Ohmeda Inc |
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