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

GS-220 HAND IMPAIRMENT EVALUATION SYSTEM

K Number: K912526 · Decision Sep 5, 1991
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
35
Applicant Total
5
Review Days
90

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Basic Information

Device Name
GS-220 HAND IMPAIRMENT EVALUATION SYSTEM
K Number
K912526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1240
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
J-Tech, Inc.
Date Received
June 7, 1991
Decision Date
September 5, 1991
Product Code
LBB
Advisory Committee
Orthopedic
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LBB Dynamometer, Ac-Powered

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K945630 LARGE MUSCLE STRENGTH GAUGE
K913587 JTECH 50 SERIES CUTTING LOOP