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

MICROLITE TUBE LUMINOMETER #011-902-0000

K Number: K890502 · Decision Feb 27, 1989
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
44
Review Days
26

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Basic Information

Device Name
MICROLITE TUBE LUMINOMETER #011-902-0000
K Number
K890502
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Dynatech Laboratories, Inc.
Date Received
February 1, 1989
Decision Date
February 27, 1989
Product Code
JJQ
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
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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K923456 MICROLITE MICROTITER PLATE LUMINOMETER ML3000
K915896 MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI
K920888 MICROLITE MICROTITER PLATE LUMINOMETER ML2200
K913590 MICROLITE ML 1000 MICROTITER PLATE LUMINOMETER
K895313 MICROLITE ML 1000 (MODEL 3) MICROPLATE LUMINOMETER
K894645 IMMULON 1,2,3,AND 4 DIVIDASTRIPS TM
K894687 DYNATECH MR 5000, CATALOG #011-976-0600
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