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

QUICKIE RX PRESCRIPTION WHEELCHAIR

K Number: K870476 · Decision Feb 26, 1987
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
445
Applicant Total
4
Review Days
23

Basic Information

Device Name
QUICKIE RX PRESCRIPTION WHEELCHAIR
K Number
K870476
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
MOTION DESIGNS, INC.
Date Received
February 3, 1987
Decision Date
February 26, 1987
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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K Number Device Name
K890050 ZIPPIE & QUICKIE 2HP WHEELCHAIR
K880280 BREEZY WHEELCHAIR
K850536 QUICKIE WHEELCHAIRS