FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PLASTAZOTE SHOE

K Number: K801743 · Decision Aug 7, 1980
Classifications
1
FEI Numbers
203
Registration Numbers
203
Same Product Code
6
Applicant Total
11
Review Days
10

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Basic Information

Device Name
PLASTAZOTE SHOE
K Number
K801743
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Alimed, Inc.
Date Received
July 28, 1980
Decision Date
August 7, 1980
Product Code
KNP
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
KNP Orthosis, Corrective Shoe

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K963526 STRAP WEDGE
K920487 MINI VIBRATOR
K840156 PROTECTA COAT SPONGES
K822650 SUPER DONUT
K822651 TOTAL FINGER FLEXION SPLINT
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K791189 ECHO CARDIOGRAM PAD
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