Medical Device Recalls
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1 result found
510(K) Number: K052135 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Gyrus CyberWand Ultrasonic Lithotripter System includes: CW-USLS CyberWand USL System CW-USLT Cyb... | 2 | 08/09/2007 |
FEI # 3003790304 Gyrus ACMI Corporation |
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