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

LUMICON

K Number: K873893 · Decision Jan 5, 1988
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
16
Review Days
104

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Basic Information

Device Name
LUMICON
K Number
K873893
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hamilton Co.
Date Received
September 23, 1987
Decision Date
January 5, 1988
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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K892369 MULTI-PROBE HEAD PLUS
K871945 MICROLAB AT
K832205 PRECISION LIQUID DISPENSER
K832202 PB 600 REPEATING DISPENSER
K832204 MICROLAB P
K832201 CHROM-PREP
K832200 PRP-1 REVERSED PHASE COLUMNS FOR HPLC
K832199 HC40/HC75 CATION EXCHANGE RESIN
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