FDA PMA FDA Class 3 Approved 🇺🇸 United States

Device, Thermal Ablation, Endometrial

PMA: P000040 · Supplement: S005 · Decision Jul 12, 2005
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Device, Thermal Ablation, Endometrial
Trade Name
HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM
PMA Number
P000040
Supplement Number
S005
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
July 12, 2005
Date Received
June 20, 2005
Supplement Type
Special (Immediate Track)
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR MANUFACTURING PROCESS AND QUALITY CONTROL CHANGES TO THE ADAPTERS USED TO CONNECT A HYSTEROSCOPE TO THE HTA SYSTEM PROCEDURE SHEATH.

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