Lumex, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K963674LUMEX AIRJanuary 10, 1997
K962123AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEMJuly 18, 1996
K953675ALTADYNESeptember 28, 1995
K945175MECHANICAL WHEELCHAIR 890.3850May 12, 1995
K945257577ES (ERGOSENSE)April 26, 1995
K944574LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)October 17, 1994
K923977AKROTECH 4000February 12, 1993
K895740SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CARTFebruary 22, 1990