Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K981269 |
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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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PRO5100, PowerPro Battery Modular Handpiece. Drill mode Nominal Speed Range: 0-1250 rpm, PRO5200... | 1 | 10/01/2009 | Linvatec Corp. dba ConMed Linvatec |
Mpower PRO6200 Single Trigger Modular Handpiece, Mpower PRO6202 Battery Two-Trigger Modular Han... | 1 | 10/01/2009 | Linvatec Corp. dba ConMed Linvatec |
PowerProMax PRO5100M Battery Single Trigger, PowerProMax PRO5200M Battery Two Trigger, PowerPr... | 1 | 10/01/2009 | Linvatec Corp. dba ConMed Linvatec |
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