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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K991522
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FHC MicroTargeting Electrode, MTDWBP(AR)(MP I ) Intended for use in intra-operative recording of ... 2 12/18/2008 FEI # 3002250546
FHC, Inc.
FC400SP microTargeting StimPilot Single Procedure Kit Distributed by Medtronic Inc., Minneapolis, ... 2 12/18/2008 FEI # 3002250546
FHC, Inc.
FC4000 MicroTargeting Electrode Kit 5x For use with Nexframe® and Nexdrive® Distributed by Medtro... 2 12/18/2008 FEI # 3002250546
FHC, Inc.
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