FDA 510(k), K091100, MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

FDA 510(k), K091100, MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

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510(K) Number: K091100
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: 04/16/2009
Decision Date: 10/23/2009
Regulation Medical Specialty: Obstetrics/Gynecology

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