Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K850054 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Angiotensin I [125I] Radioimmunoassay Kit, 500 Tube Catalog Number: NEA105 For in-vitro diagnostic... | 2 | 09/12/2003 | Perkinelmer Life Sciences, Inc. |
| Angiotensin I [125I] Radioimmunoassay Kit, 250 Tube Catalog Number: NEA104 For in-vitro diagnostic... | 2 | 09/12/2003 | Perkinelmer Life Sciences, Inc. |
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