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FDA 510(k), K142029, MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
FDA 510(k), K142029, MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
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510(K) Number: K142029
Device Name: MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
Manufacturer: HOLOGIC, INC.
Device Classification Name: hysteroscope (and accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 07/25/2014
Decision Date: 11/26/2014
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
Manufacturer: HOLOGIC, INC.
Device Classification Name: hysteroscope (and accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 07/25/2014
Decision Date: 11/26/2014
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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