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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K912492
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Endopath Probe Plus II, Hook Electrode, 5 mm Shaft, 34 cm length, hollow tip electrdode, Product Cod... 2 05/31/2006 Ethicon Endo-Surgery Inc
Endopath Probe Plus II, Foot-Controlled PistolGrip Handle, Product Code EPH01. 2 05/31/2006 Ethicon Endo-Surgery Inc
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