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UROLOGIX TARGIS SYSTEM

FDA premarket approval P970008/S014 · decided 2000-03-02

Approval details

PMA number
P970008
Supplement
S014
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
UROLOGIX TARGIS SYSTEM
Generic name
System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
Applicant
Urologix, LLC
Date received
2000-01-19
Decision date
2000-03-02
Days to decision
43 days
Decision code
APPR
Product code
MEQ
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Plymouth, MN
Statement
Approval for a modification to the software to add the auto-control option to the Targis System treatment.

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