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

LYRIS 100/120 LABORATORY INFORMATION SYSTEM

K Number: K923844 · Decision Dec 11, 1992
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
11
Review Days
133

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Basic Information

Device Name
LYRIS 100/120 LABORATORY INFORMATION SYSTEM
K Number
K923844
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biovation, Inc.
Date Received
July 31, 1992
Decision Date
December 11, 1992
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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K812604 BIOVATION URINALYSIS REPORTER
K792045 BIOVATION NEPHELOMETER
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K781644 ANTIBIOTIC NEPHELOMETER
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