FDA PMA FDA Class 3 Approved 🇺🇸 United States

Device, Thermal Ablation, Endometrial

PMA: P010013 · Supplement: S012 · Decision Mar 24, 2005
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Device, Thermal Ablation, Endometrial
Trade Name
NOVASURE GLOBAL IMPENDENCE CONTROLLED ENDOMETRIAL ABLATION SYSTEM
PMA Number
P010013
Supplement Number
S012
Device Class
FDA Class 3
Product Code
MNB
Generic Name
Device, thermal ablation, endometrial
Medical Specialty
Unknown
Advisory Committee
Obstetrics/Gynecology
Decision
Approved
Decision Code
APPR
Decision Date
March 24, 2005
Date Received
October 25, 2004
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A MANUFACTURING SITE LOCATED AT CYTYC SURGICAL PRODUCTS, HEREDIA, COSTA RICA.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MNB Device, Thermal Ablation, Endometrial