Atlas FDA

PROSTATRON

FDA premarket approval P950014/S003 · decided 1996-12-27

Approval details

PMA number
P950014
Supplement
S003
Supplement type
Normal 180 Day Track
Supplement reason
Other
Trade name
PROSTATRON
Generic name
System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
Applicant
Urologix, Inc.
Date received
1996-09-23
Decision date
1996-12-27
Days to decision
95 days
Decision code
APPR
Product code
MEQ
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Plymouth, MN
Statement
APPROVAL FOR CHANGES TO THE PROSTATRON(TM) POSTAPPROVAL STUDY CASE REPORT FORM.

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510(k) clearances by this applicant

RecordFirmDate
Prostiva RF Therapy Generator, Prostiva RF Therapy Hand Piece, Prostiva RF Therapy Return Electrode, Prostiva RF Therapy Tubing System, Prostiva RF Therapy Telescope (K142248)Urologix, Inc.2015-02-20