FDA 510(k), K120593, MYOSURE CONTROL UNIT

FDA 510(k), K120593, MYOSURE CONTROL UNIT

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510(K) Number: K120593
Device Name: MYOSURE CONTROL UNIT
Manufacturer:
Device Classification Name: Hysteroscope (And Accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 02/28/2012
Decision Date: 03/23/2012
Regulation Medical Specialty: Obstetrics/Gynecology
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