• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K063367, 45L CORE INSUFFLATOR, MODEL F114, by W.O.M. World of Medicine AG

FDA 510(k) K063367, 45L CORE INSUFFLATOR, MODEL F114, by W.O.M. World of Medicine AG

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510(K) Number: K063367
Device Name: 45L CORE INSUFFLATOR, MODEL F114
Manufacturer: W.O.M. World of Medicine AG
Device Classification Name: insufflator, laparoscopic
Regulation Number: 884.1730
Classification Product Code: HIF
Date Received: 11/07/2006
Decision Date: 05/23/2007
Regulation Medical Specialty: Obstetrics/Gynecology
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