PMA P870043S011

Device
2.5 HOLIUM/ND:YAG SPECTRAPROBE FLEX CATHETER
Applicant
Trimedyne, Inc.
PMA number
P870043
Supplement
S011
Product code
LPC
Decision date
1990-11-14
Classification
Device, Angioplasty, Laser, Coronary
Generic name
DEVICE, ANGIOPLASTY, LASER, CORONARY

Current openFDA PMA Record#

Device
2.5 HOLIUM/ND:YAG SPECTRAPROBE FLEX CATHETER
Applicant
Trimedyne, Inc.
PMA number
P870043
Supplement
S011
Product code
LPC
Generic name
DEVICE, ANGIOPLASTY, LASER, CORONARY
Decision date
1990-11-14
Decision code
APPR
Date received
1990-04-30
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material