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FDA 510(k), K172566, Myosure Hysteroscopic Tissue Removal System and Myosure Tissue Removal Devices
FDA 510(k), K172566, Myosure Hysteroscopic Tissue Removal System and Myosure Tissue Removal Devices
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510(K) Number: K172566
Device Name: Myosure Hysteroscopic Tissue Removal System and Myosure Tissue Removal Devices
Manufacturer: Hologic, Inc.
Device Classification Name: Hysteroscope (And Accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 08/25/2017
Decision Date: 09/20/2017
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: Myosure Hysteroscopic Tissue Removal System and Myosure Tissue Removal Devices
Manufacturer: Hologic, Inc.
Device Classification Name: Hysteroscope (And Accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 08/25/2017
Decision Date: 09/20/2017
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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