FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

LERADO, POWER WHEELCHAIR, PB

K Number: K070433 · Decision Mar 16, 2007
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
6
Review Days
30

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Basic Information

Device Name
LERADO, POWER WHEELCHAIR, PB
K Number
K070433
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lerado China Limited
Date Received
February 14, 2007
Decision Date
March 16, 2007
Product Code
ITI
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
ITI Wheelchair, Powered

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