FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)

K Number: K944574 · Decision Oct 17, 1994
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
8
Review Days
28

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Basic Information

Device Name
LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)
K Number
K944574
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lumex, Inc.
Date Received
September 19, 1994
Decision Date
October 17, 1994
Product Code
IOR
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IOR Wheelchair, Mechanical

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Other Clearances by Lumex, Inc.

K Number Device Name
K963674 LUMEX AIR
K962123 AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM
K953675 ALTADYNE
K945175 MECHANICAL WHEELCHAIR 890.3850
K945257 577ES (ERGOSENSE)
K923977 AKROTECH 4000
K895740 SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART