Atlas FDA

MICROSULIS MICROWAVE ENDOMETERIAL ABLATION (MEA) SYSTEM

FDA premarket approval P020031/S001 · decided 2005-05-25

Approval details

PMA number
P020031
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MICROSULIS MICROWAVE ENDOMETERIAL ABLATION (MEA) SYSTEM
Generic name
Device, thermal ablation, endometrial
Applicant
Microsulis Medical , Ltd.
Date received
2004-03-09
Decision date
2005-05-25
Days to decision
442 days
Decision code
APPR
Product code
MNB
Advisory committee
Obstetrics/Gynecology
Expedited review
No
Location
Denmead Hampshire
Statement
APPROVAL FOR THE SINGLE USE MEA APPLICATOR.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.