FDA 510(k), K081070, INTERLACE MEDICAL OPERATIVE HYSTEROSCOPY SYSTEM

FDA 510(k), K081070, INTERLACE MEDICAL OPERATIVE HYSTEROSCOPY SYSTEM

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510(K) Number: K081070
Device Name: INTERLACE MEDICAL OPERATIVE HYSTEROSCOPY SYSTEM
Manufacturer:
Device Classification Name: Hysteroscope (And Accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 04/15/2008
Decision Date: 07/23/2008
Regulation Medical Specialty: Obstetrics/Gynecology
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