• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K100559, MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM, by Interlace Medical, Inc.

FDA 510(k) K100559, MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM, by Interlace Medical, Inc.

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510(K) Number: K100559
Device Name: MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
Manufacturer: Interlace Medical, Inc.
Device Classification Name: hysteroscope (and accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 03/01/2010
Decision Date: 03/30/2010
Regulation Medical Specialty: Obstetrics/Gynecology
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