Atlas FDA

SCIMED WAVE

FDA premarket approval P860019/S109 · decided 1996-02-05

Approval details

PMA number
P860019
Supplement
S109
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
SCIMED WAVE
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Scimed Life Systems, Inc.
Date received
1995-12-22
Decision date
1996-02-05
Days to decision
45 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
APPROVAL FOR THE USE OF AN EPOXY ADHESIVE IN THE MANIFOLD OF THE BANDIT, POC BANDIT, AND THE 15 MM NC BANDIT PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY CATHETERS

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
SCIMED INFORMER PRESSURE WIRE SYSTEM (K974241)Scimed Life Systems, Inc.1998-11-12
SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETER (K981788)Scimed Life Systems, Inc.1998-08-18
SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRES (K980360)Scimed Life Systems, Inc.1998-04-29
SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS (K974559)Scimed Life Systems, Inc.1998-02-23
SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETER (K974684)Scimed Life Systems, Inc.1998-02-19
LUGE GUIDE WIRE (K973945)Scimed Life Systems, Inc.1998-01-12
SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER (K970823)Scimed Life Systems, Inc.1997-06-03
CHOICE SUPER SUPPORT PTCA GUIDE WIRE, CHOICE PLUS SUPER SUPPORT PTCA GUIDE WIRE, CHOICE EXCHANGE SUPER SUPPORT PTCA GUID (K964551)Scimed Life Systems, Inc.1997-05-21