Medical Device Recalls
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1 result found
510(K) Number: K933334 |
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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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Medi-Tech Magic Torque Glidex hydrophilic coated guidewire, .035 inch/180 cm and .035 inch/260 cm le... | 3 | 03/20/2003 | Symbiosis Corp. |
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