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

PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER

K Number: K870777 · Decision Mar 13, 1987
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
56
Applicant Total
12
Review Days
15

Basic Information

Device Name
PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER
K Number
K870777
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2170
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
KONE INSTRUMENTS, INC.
Date Received
February 26, 1987
Decision Date
March 13, 1987
Product Code
JJF
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
JJF Analyzer, Chemistry, Micro, For Clinical Use

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K Number Device Name
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K860767 MODEL E 600 ELECTROCARDIOGRAPH
K853354 MEDIC 4
K840200 PROGRESS SELECTIVE DHEMISTRY ANALYZ
K830432 CENTRAL STATION 590
K830433 PATIENT MONITOR 575
K822952 560
K820541 MICROLYTE
Search all 12 clearances from KONE INSTRUMENTS, INC. →