Medical Device Recalls
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1 result found
510(K) Number: K152464 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD... | 2 | 04/21/2022 |
FEI # 3003742580 DNA Genotek Inc. |
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