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

GELSCAN SOFTWARE 2190

K Number: K834490 · Decision May 1, 1984
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
77
Applicant Total
52
Review Days
147

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Basic Information

Device Name
GELSCAN SOFTWARE 2190
K Number
K834490
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
December 6, 1983
Decision Date
May 1, 1984
Product Code
JQP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JQP Calculator/Data Processing Module, For Clinical Use

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