Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K121864 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended... | 3 | 07/24/2017 |
FEI # 3007145015 PerkinElmer Health Sciences, Inc. |
| PerkinElmer 226 Sample Collection Device | 3 | 06/04/2020 |
FEI # 3007145015 PerkinElmer Health Sciences, Inc. |
| Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 2... | 2 | 10/18/2013 |
FEI # 3007145015 Perkin Elmer Health Sciences, Inc. |
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