Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K110779 |
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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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Spacelabs Smart Disclosure System, Model 92810, is an integrated component of the Intesys Clinical S... | 2 | 01/17/2013 | Spacelabs Healthcare, Llc |
Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite... | 2 | 07/22/2019 | Spacelabs Healthcare, Inc. |
Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11 Rev A and Update Kit, PN:... | 2 | 03/25/2014 | Spacelabs Healthcare, Llc |
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