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

IMMOBILINE SYSTEM LKB 1819

K Number: K830797 · Decision Aug 24, 1983
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
33
Applicant Total
52
Review Days
163

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Basic Information

Device Name
IMMOBILINE SYSTEM LKB 1819
K Number
K830797
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
March 14, 1983
Decision Date
August 24, 1983
Product Code
JJN
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
JJN Apparatus, Electrophoresis, For Clinical Use

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K871599 DELFIA(TM) HIGE KIT
K871644 DELFIA (TM) HTSH KIT
K864452 DELFIA(TM) TRIIODOTHYRONINE (T3) KIT
K864733 LKB 2260 MACROTOME
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K863422 DELFIA(TM) CORTISOL KIT
K861195 DELFIA DIGOXIN
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