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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K925903
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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ABC PROBE REF 160656 5 mm Handswitching Probe, 28 cm QTY: 1 STERILE CONMED CORPORATION 525 FRENCH RD... 2 08/25/2010 ConMed Electrosurgery
ABC PROBE REF 160655 5 mm Footswitching Probe, QTY: 1 STERILE CONMED CORPORATION 525 French Rd, Uti... 2 08/25/2010 ConMed Electrosurgery
ABC PROBE REF 160644 5 mm Handswitching Probe, 44 cm QTY: 1 STERILE CONMED CORPORATION 525 French R... 2 08/25/2010 ConMed Electrosurgery
ABC PROBE REF 160636 5 mm Handswitching Probe, 36 cm QTY: 1 STERILE CONMED CORPORATION 525 French Rd... 2 08/25/2010 ConMed Electrosurgery
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