FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇳 China

Manual Wheelchair

K Number: K180852 · Decision Mar 1, 2019
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
1
Review Days
333

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Basic Information

Device Name
Manual Wheelchair
K Number
K180852
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jiangyin Newrise Medical Equipment Co., Ltd.
Date Received
April 2, 2018
Decision Date
March 1, 2019
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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