Meadox Surgimed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MS CLASSIQUE BALLOON CATHETER, NOPROFILE OLBERT CATHETER SYSTEM, MS AMPLATZ EXTRA STIFF GUIDE WIRE
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Meadox Surgimed, Inc. Gastroenterology & Urology ✕
14 devices
Cleared
Mar 13, 1995
MS CLASSIQUE BALLOON CATHETER
Gastroenterology & Urology
200d
Cleared
Mar 09, 1995
NOPROFILE OLBERT CATHETER SYSTEM
Gastroenterology & Urology
146d
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
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
Feb 12, 1987
CYTOSTATIC FILTRATION SET
Gastroenterology & Urology
176d
Cleared
Jan 20, 1987
UROCUT BIOPSY NEEDLE
Gastroenterology & Urology
291d
Cleared
Oct 31, 1986
NEPHROSTOMY SET
Gastroenterology & Urology
102d
Cleared
May 19, 1986
LUNDERQUIST - RING PTC DRAINAGE CATHETER
Gastroenterology & Urology
48d
Cleared
Dec 02, 1985
ROTEX SCREW BIOPSY NEEDLE
Gastroenterology & Urology
31d
Cleared
Jul 03, 1985
OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO
Gastroenterology & Urology
72d
Cleared
May 23, 1985
OLBERT CATHETER SYS FOR URETERAL DILATION
Gastroenterology & Urology
38d