Rms Div.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K963367RMS K-WIREOctober 30, 1996
K954438SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPEDecember 29, 1995
K944848THE VIVACARE T.P.S. PROBEDecember 14, 1994
K944557DW250 #91November 3, 1994
K941625DW234 #29June 22, 1994
K902403ELITE R/F SPOT FILM DRIVEAugust 1, 1990
K902146SFD-035 SPOT FILM DEVICEMay 31, 1990
K896665EXT-600 TABLE, RADIOGRAPHIC, ELEVATINGJanuary 22, 1990
K896119RMS 90/15 RADIOGRAPHIC/FLUOROSCOPIC TILTING TABLENovember 27, 1989
K896324ELITE 1500 RADIOGRAPHIC TILTING TABLENovember 21, 1989