Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K102239 |
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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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| GE Healthcare, CARESCAPE Monitor B650. A multi-parameter patient monitor intended for use in multipl... | 2 | 07/24/2014 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239 CARESCAPE Monitor B650 T... | 2 | 03/11/2014 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The CARESCAPE Monitor B650 is a ... | 2 | 01/28/2014 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare, CARESCAPE Monitor B650. The CARESCAPE Monitor B650 is a multi-parameter patient mo... | 2 | 09/19/2013 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare, CARESCAPE Monitor B650. The CARESCAPE Monitor B650 is a multi-parameter patient mo... | 2 | 02/14/2013 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare, CARESCAPE Monitor B650 The CARESCAPE Monitor B650 is a multi-parameter patient mon... | 2 | 04/08/2011 |
FEI # 2126677 GE Healthcare, LLC |
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