PMA P160047S005

Device
MARA Water Vapor System
Applicant
CooperSurgical, Inc.
Product code
MNB
Decision date
2020-01-08
Generic name
Device, thermal ablation, endometrial
Approval order statement
Approval of changes to the instructions for use and patient labeling to include the results of the Post-Ablation Cavity Evaluation (PACE) study, which evaluated the ability to assess the uterine cavity more than three-years post endometrial ablation with the MARA Water Vapor System

Current openFDA PMA Record#

Device
MARA Water Vapor System
Applicant
CooperSurgical, Inc.
PMA number
P160047
Supplement
S005
Product code
MNB
Generic name
Device, thermal ablation, endometrial
Decision date
2020-01-08
Decision code
APPR
Date received
2019-06-19
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Approval order statement
Approval of changes to the instructions for use and patient labeling to include the results of the Post-Ablation Cavity Evaluation (PACE) study, which evaluated the ability to assess the uterine cavity more than three-years post endometrial ablation with the MARA Water Vapor System