Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Hysteroscope (And Accessories)
510(k) Number K142029
Device Name MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
Applicant
Hologic, Inc.
250 Campus Dr.
Marlborough,  MA  01752
Applicant Contact SARAH FAIRFIELD
Correspondent
Hologic, Inc.
250 Campus Dr.
Marlborough,  MA  01752
Correspondent Contact SARAH FAIRFIELD
Regulation Number884.1690
Classification Product Code
HIH  
Date Received07/25/2014
Decision Date 11/26/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-