Atlas FDA

SCIMED(R) PTCA CATHETER

FDA premarket approval P860019/S094 · decided 1995-12-07

Approval details

PMA number
P860019
Supplement
S094
Supplement type
Normal 180 Day Track
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SCIMED(R) PTCA CATHETER
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Scimed Life Systems, Inc.
Date received
1994-10-05
Decision date
1995-12-07
Days to decision
428 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
APPROVAL FOR A CHANGE IN STERILIZATION PROCESS FROM 12/88 ETHYLENE OXIDE/CFC-12 TO 8.6/91.6 OXYFUME 2000 MIXTURE

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