Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K010599 |
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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; PROTIME CUVETTE AND PROTIME3 CUVETTE; Store the foil-pouched cuvett... | 2 | 09/13/2013 |
FEI # 3009929723 Assuramed |
| Pro Time Microcoagulation System/ Pro Time 3 Cuvette, Pro3-4, Pro3-25, and Pro3-50. International T... | 2 | 02/19/2013 |
FEI # 1000526865 International Technidyne Corp. |
| ProTime Microcoagulation System Instrument, Catalogue Number: PROTIMEPRO, International Technidyne C... | 2 | 01/25/2008 |
FEI # 3005776351 International Technidyne Corporation |
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