Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K951072 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ProTime Microcoagulation System Instrument:Catalogue Number: PROTIMEINT, International Technidyne ... | 2 | 01/25/2008 | International Technidyne Corporation |
| International Technidyne Corporation (ITC) ProTime Microcoagulation System Instrument-Catalogue Numb... | 3 | 01/13/2007 | International Technidyne Corp. |
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