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

LYRIS MODULAR INFO SYSTEM

K Number: K831830 · Decision Jun 25, 1984
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
77
Applicant Total
11
Review Days
384

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Basic Information

Device Name
LYRIS MODULAR INFO SYSTEM
K Number
K831830
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biovation, Inc.
Date Received
June 7, 1983
Decision Date
June 25, 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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Other Clearances by Biovation, Inc.

K Number Device Name
K925528 BIOVATION K-MANAGER
K923844 LYRIS 100/120 LABORATORY INFORMATION SYSTEM
K915071 DIFFERENTIAL COUNTING BOARD
K853026 BIOVATION MAX DATA MANAGEMENT SYSTEM
K842401 CHEMISTRY CONSOLE
K821534 HEMATOLOGY DATA MANAGEMENT SYS
K812604 BIOVATION URINALYSIS REPORTER
K792045 BIOVATION NEPHELOMETER
K790862 BIOVATION DIGITAL URINOMETER
K781644 ANTIBIOTIC NEPHELOMETER
Search all 11 clearances from Biovation, Inc. →