Meadox Surgimed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meadox Surgimed, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Meadox Surgimed, Inc. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1984 to 1995. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Meadox Surgimed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meadox Surgimed, Inc.
24 devices
Cleared
Mar 13, 1995
MS CLASSIQUE BALLOON CATHETER
Gastroenterology & Urology
200d
Cleared
Mar 09, 1995
NOPROFILE OLBERT CATHETER SYSTEM
Gastroenterology & Urology
146d
Cleared
Aug 22, 1994
MS AMPLATZ EXTRA STIFF GUIDE WIRE
Cardiovascular
95d
Cleared
Jun 09, 1993
ACECUT SUTOMATIC BIOPSY SYSTEM
Gastroenterology & Urology
146d
Cleared
Jun 20, 1991
MEADOX(R) SURGIMED(R) BIOPSY GUN II
Gastroenterology & Urology
70d
Cleared
Mar 06, 1991
NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY
Gastroenterology & Urology
107d
Cleared
Feb 25, 1991
QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE
Cardiovascular
139d
Cleared
Jan 30, 1991
MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGY
Gastroenterology & Urology
89d
Cleared
Jul 16, 1990
MEADOX SURGIMED BIOPSY GUN AND NEEDLE
Gastroenterology & Urology
42d
Cleared
Jun 20, 1989
SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE
General Hospital
116d
Cleared
Feb 12, 1987
CYTOSTATIC FILTRATION SET
Gastroenterology & Urology
176d
Cleared
Jan 20, 1987
UROCUT BIOPSY NEEDLE
Gastroenterology & Urology
291d