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

OPTIMA

K Number: K011053 · Decision Apr 20, 2001
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
19
Review Days
14

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Basic Information

Device Name
OPTIMA
K Number
K011053
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medical Industries America, Inc.
Date Received
April 6, 2001
Decision Date
April 20, 2001
Product Code
ITI
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
Y

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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K942444 3002 AEROMAX
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