ClearanceBrief
Company ยท US

Lumex, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1997. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FNMMattress, Air Flotation, Alternating Pressure3
IORWheelchair, Mechanical2
FPOStretcher, Wheeled1
INOChair, Positioning, Electric1
IOQBed, Flotation Therapy, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 10, 1997K963674LUMEX AIR
Lumex, Inc.
FNM
Jul 18, 1996K962123AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM
Lumex, Inc.
FNM
Sep 28, 1995K953675ALTADYNE
Lumex, Inc.
FNM
May 12, 1995K945175MECHANICAL WHEELCHAIR 890.3850
Lumex, Inc.
IOR
Apr 26, 1995K945257577ES (ERGOSENSE)
Lumex, Inc.
INO
Oct 17, 1994K944574LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)
Lumex, Inc.
IOR
Feb 12, 1993K923977AKROTECH 4000
Lumex, Inc.
IOQ
Feb 22, 1990K895740SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART
Lumex, Inc.
FPO

Latest recalls

DateFirm and productCodeLinked 510(k)
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