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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K022051
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Product Description
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FDA Recall
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Linemaster Wireless Footswitch, VASER System, REF Vaser 2.0, Sound Surgical Technologies LLC, 357 So... 2 01/25/2011 Sound Surgical Technologies, LLC
Linemaster Wireless Footswitch Accessory, Model SP-9970214-005112010 and Model SP-9970214-005112232.... 2 03/13/2008 Sound Surgical Technologies, LLC