Medical Device Manufacturer · US , Mchenry , IL

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

24 submissions · 24 cleared · Since 1984

Recent clearances: MS CLASSIQUE BALLOON CATHETER, NOPROFILE OLBERT CATHETER SYSTEM, MS AMPLATZ EXTRA STIFF GUIDE WIRE

View 24 510(k) Devices ↓

24

Total

24

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Jun 20, 1989

SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE

General Hospital · 116d

Cleared Jun 28, 1984

THINWALL PUNCTURE NEEDLE

General Hospital · 66d