Lumex, Inc.
Lumex, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1997.
Top product codes for Lumex, Inc.
Recent clearances by Lumex, Inc.
- K963674 — LUMEX AIR
- K962123 — AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM
- K953675 — ALTADYNE
- K945175 — MECHANICAL WHEELCHAIR 890.3850
- K945257 — 577ES (ERGOSENSE)
- K944574 — LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)
- K923977 — AKROTECH 4000
- K895740 — SHOWER CHAIRS; BED/STRETCHER; LINEN & UTILITY CART
Data sourced from openFDA. This site is unofficial and independent of the FDA.