Medical Device Manufacturer · US , Mchenry , IL

Meadox Surgimed, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1984

24

Total

24

Cleared

0

Denied

FDA 510(k) Regulatory Record - Meadox Surgimed, Inc. Cardiovascular ✕

6 devices

1-6 of 6

Cleared Aug 22, 1994

MS AMPLATZ EXTRA STIFF GUIDE WIRE

Cardiovascular · 95d

Cleared Feb 25, 1991

QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE

Cardiovascular · 139d

Cleared Sep 02, 1986

OLBERT CATHETER SYSTEM WITH SIDEWINDER CURVE

Cardiovascular · 61d

Cleared Jul 18, 1986

THE NAVIGATOR STEERABLE GUIDE WIRE

Cardiovascular · 164d

Cleared Apr 23, 1986

MEADOX SURGIMED GUIDE CATHETER

Cardiovascular · 78d

Cleared Dec 27, 1984

MEADOX SURGIMED A/S CATHETER SHEATH SYS

Cardiovascular · 91d