Medical Device Recalls
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1 result found
510(K) Number: K002343 |
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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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Delta Vaporizer An anesthetic vaporizer is a device used to vaporize liquid anesthetic and delive... | 2 | 07/02/2013 | Penlon, Ltd. |
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