Medical Device Recalls
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1 result found
510(K) Number: K990897 |
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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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| Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The inten... | 2 | 01/24/2014 |
FEI # 2936999 Nellcor Puritan Bennett Inc. (dba Covidien LP) |
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