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ACS RX ESPRIT CORONARY DILATION CATHETER

FDA premarket approval P810046/S189 · decided 1998-06-27

Approval details

PMA number
P810046
Supplement
S189
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ACS RX ESPRIT CORONARY DILATION CATHETER
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Advanced Cardiovascular Systems, Inc.
Date received
1998-04-30
Decision date
1998-06-27
Days to decision
58 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Temecula, CA
Statement
Approval for an alternate E-beam sterilization facility located at Titan Scan Systems, 9020 Activity Rd., Suite D, San Diego, CA 92126.

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510(k) clearances by this applicant

RecordFirmDate
HI-TORQUE MIDDLE SUPPORT .012 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING (K012534)Advanced Cardiovascular Systems, Inc.2002-01-24
OTW MEGALINK SDS BILIARY STENT SYSTEM (K000550)Advanced Cardiovascular Systems, Inc.2000-03-17
VERIPATH PERIPHERAL GUIDING CATHETER (K994229)Advanced Cardiovascular Systems, Inc.2000-02-25
ACS HI-TORQUE CROSS-IT 400XT GUIDE WIRE (K992169)Advanced Cardiovascular Systems, Inc.1999-10-28
RX HERCULINK 14 BILIARY STENT SYSTEM, MODEL 1005126-18,1005128-18,1005130-18,1005132-18,1005134-18,1005136-18,1005138-18 (K990867)Advanced Cardiovascular Systems, Inc.1999-09-02
ACS HI-TORQUE IRON MAN GUIDE WIRE (K963702)Advanced Cardiovascular Systems, Inc.1997-01-22
INDEFLATOR PLUS 30/PLUS 30 PRIORITY PACK9WITH THE.096 OR.115 ROTATING HEMOSTATIC VALVE) (K962495)Advanced Cardiovascular Systems, Inc.1996-09-12
INDEFLATOR 20/30 INFLATION DEVICE AND 20/30 PRIORITY PACK (WITH THE .096 OR .115 ROTATING HEMOSTATIC VALVE) (K961471)Advanced Cardiovascular Systems, Inc.1996-05-08