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INGClass II

Elevator, Wheelchair, Portable

21 CFR 890.3930 / Physical Medicine

ING is the FDA product code for Elevator, Wheelchair, Portable, a class II device type, regulated under 21 CFR 890.3930. FDA's definition for this code reads: "A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs)". As of , FDA records hold 29 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
ING
Device name
Elevator, Wheelchair, Portable
FDA definition
A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs).
Regulation
21 CFR 890.3930
Device class
Class II
Review panel
Physical Medicine
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
29
Ingested recalls
3

Clearances, product code ING

By decision year
29 clearances under product code ING with a decision year between 1985 and 2012, 1990 the highest year at 6.
Show the numbers
510(k) clearances under FDA product code ING by decision year
YearClearances
19851
19892
19906
19922
19942
19951
19963
19982
20021
20031
20041
20061
20081
20092
20101
20111
20121

Applicants with the most clearances

Product code ING

Companies listing this code with FDA

Companies whose registered establishments list this code