Atlas FDA

LASTAC SYSTEM

FDA premarket approval P870071/S001 · decided 1989-02-02

Approval details

PMA number
P870071
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
LASTAC SYSTEM
Generic name
DEVICE, ANGIOPLASTY, LASER, CORONARY
Applicant
G V Medical, Inc.
Date received
1988-12-12
Decision date
1989-02-02
Days to decision
52 days
Decision code
APPR
Product code
LPC
Advisory committee
Cardiovascular
Expedited review
No
Location
Minneapolis, MN

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510(k) clearances by this applicant

RecordFirmDate
GV MEDICAL, INC. LASTAC BALLOON DILATATION CATHETE (K851080)G V Medical, Inc.1985-06-20