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Meadox Surgimed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K944143MS CLASSIQUE BALLOON CATHETERMarch 13, 1995
K945061NOPROFILE OLBERT CATHETER SYSTEMMarch 9, 1995
K942382MS AMPLATZ EXTRA STIFF GUIDE WIREAugust 22, 1994
K930201ACECUT SUTOMATIC BIOPSY SYSTEMJune 9, 1993
K911635MEADOX(R) SURGIMED(R) BIOPSY GUN IIJune 20, 1991
K905181NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGYMarch 6, 1991
K904582QUICKWIRE - HYDROPHILIC COATED GUIDEWIREFebruary 25, 1991
K904983MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGYJanuary 30, 1991
K902461MEADOX SURGIMED BIOPSY GUN AND NEEDLEJuly 16, 1990
K890926SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLEJune 20, 1989
K863218CYTOSTATIC FILTRATION SETFebruary 12, 1987
K861267UROCUT BIOPSY NEEDLEJanuary 20, 1987
K862742NEPHROSTOMY SETOctober 31, 1986
K862550OLBERT CATHETER SYSTEM WITH SIDEWINDER CURVESeptember 2, 1986
K860430THE NAVIGATOR STEERABLE GUIDE WIREJuly 18, 1986
K861220LUNDERQUIST - RING PTC DRAINAGE CATHETERMay 19, 1986
K860429MEADOX SURGIMED GUIDE CATHETERApril 23, 1986
K854262MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLYDecember 24, 1985
K854404ROTEX SCREW BIOPSY NEEDLEDecember 2, 1985
K854420MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDLNovember 22, 1985