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 | SPECTRAPROBE-PLR CATH. & OPTILASE/CARDIOLASE LASER |
Generic Name | DEVICE, ANGIOPLASTY, LASER, CORONARY |
Applicant | TRIMEDYNE, INC. 25901 COMMERCENTRE DR LAKE FOREST, CA 92630 |
PMA Number | P870043 |
Supplement Number | S015 |
Date Received | 08/29/1991 |
Decision Date | 03/20/1992 |
Withdrawal Date
|
08/08/2012 |
Product Code |
LPC |
Advisory Committee |
Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
|
|