FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

GAIT-AID ORTHOPEDIC INSOLE

K Number: K874502 · Decision Nov 30, 1987
Classifications
1
FEI Numbers
503
Registration Numbers
503
Same Product Code
51
Applicant Total
1
Review Days
28

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Basic Information

Device Name
GAIT-AID ORTHOPEDIC INSOLE
K Number
K874502
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Gait-Aid, Inc.
Date Received
November 2, 1987
Decision Date
November 30, 1987
Product Code
IQI
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
IQI Orthosis, Limb Brace

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