FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

QUICKIE RHYTHM & GROOVE SERIES POWER WHEELCHAIRS W/QUICKIE DELPHI CONTROLS

K Number: K060531 · Decision Mar 17, 2006
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
14
Review Days
17

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Basic Information

Device Name
QUICKIE RHYTHM & GROOVE SERIES POWER WHEELCHAIRS W/QUICKIE DELPHI CONTROLS
K Number
K060531
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sunrise Medical
Date Received
February 28, 2006
Decision Date
March 17, 2006
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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