Argon Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argon Medical Corp. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Argon Medical Corp. has 27 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1976 to 1991. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Argon Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Argon Medical Corp.
27 devices
Cleared
Jan 15, 1991
CLOSED SYSTEM FLUSH SET
Cardiovascular
69d
Cleared
Feb 28, 1990
CATHETER BALLOON DILATOR PRESSURE GAUGE
Cardiovascular
169d
Cleared
Sep 28, 1989
OBTURATOR
Cardiovascular
106d
Cleared
May 19, 1989
INTRODUCER FOR PTCA GUIDING CATHETERS
Cardiovascular
80d
Cleared
Jan 11, 1989
TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER
Cardiovascular
85d
Cleared
Aug 12, 1988
OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE
Cardiovascular
78d
Cleared
Apr 10, 1987
KADIR HI-TORQUE GUIDE WIRE
Gastroenterology & Urology
10d
Cleared
Sep 12, 1985
ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES
General & Plastic Surgery
36d
Cleared
Aug 29, 1985
PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET)
Cardiovascular
51d
Cleared
Mar 27, 1985
PATHFINDER CARDIOVASCULAR CATHETER
Cardiovascular
126d
Cleared
Jan 29, 1985
ARGON DUAL LUMEN HEMODIALYSIS, CATHETER
Gastroenterology & Urology
253d
Cleared
Jan 02, 1985
HYDROGLIDE SPRING GUIDE WIRES
Cardiovascular
237d