Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
|
Device | PROLIEVE THERMODILITATION SYSTEM |
Generic Name | System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy |
Applicant | MEDIFOCUS, INC 10240 OLD COLUMBIA ROAD SUITE G COLUMBIA, MD 21046 |
PMA Number | P030006 |
Supplement Number | S022 |
Date Received | 04/02/2009 |
Decision Date | 11/23/2009 |
Product Code |
MEQ |
Advisory Committee |
Gastroenterology/Urology |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Recalls | CDRH Recalls |
Approval Order Statement APPROVAL FOR SPECIFIC MODIFICATIONS TO THE TREATMENT CATHETER DESIGN, CATHETER MANUFACTURING PROCESSES, AND CATHETER SPECIFICATIONS. |
Post-Approval Study | Show Report Schedule and Study Progress |
|
|