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

TOTAL FINGER FLEXION SPLINT

K Number: K822651 · Decision Sep 17, 1982
Classifications
1
FEI Numbers
416
Registration Numbers
416
Same Product Code
35
Applicant Total
11
Review Days
15

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Basic Information

Device Name
TOTAL FINGER FLEXION SPLINT
K Number
K822651
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Alimed, Inc.
Date Received
September 2, 1982
Decision Date
September 17, 1982
Product Code
ILH
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
ILH Splint, Hand, And Components

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K963526 STRAP WEDGE
K920487 MINI VIBRATOR
K840156 PROTECTA COAT SPONGES
K822650 SUPER DONUT
K820516 ARTERIAL CANALIZATION DEVICE
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K791189 ECHO CARDIOGRAM PAD
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