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

QUICKIE CARBON WHEELCHAIR

K Number: K915533 · Decision Jan 22, 1992
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
4
Review Days
43

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Basic Information

Device Name
QUICKIE CARBON WHEELCHAIR
K Number
K915533
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sunrise Medical Quickie Designs, Inc.
Date Received
December 10, 1991
Decision Date
January 22, 1992
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 Sunrise Medical Quickie Designs, Inc.

K Number Device Name
K920179 ZIPPIE P500
K920463 ZIPPIE 3 TS/SP WHEELCHAIR/STANDER
K920180 QUICKIE P100