FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IL SYSTEM 1304 & 1306, PH/BLOOD GAS ANALYZERS

K Number: K852676 · Decision Jul 22, 1985
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
7
Review Days
28

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Basic Information

Device Name
IL SYSTEM 1304 & 1306, PH/BLOOD GAS ANALYZERS
K Number
K852676
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Allied Instrumentation Laboratory
Date Received
June 24, 1985
Decision Date
July 22, 1985
Product Code
CHL
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
CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

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Other Clearances by Allied Instrumentation Laboratory

K Number Device Name
K861901 MULTI-4 CO-OXIMETER CONTROL
K860365 PHENOBARBITAL TEST SYSTEM
K860286 IL TEST PHENYTOIN
K853858 IL TEST THEOPHYLLINE ASSAY
K851933 CLINICAL CHEMISTRY ANALYTICAL SYSTEM
K850748 I-L TEST, DIRECT BILIRUBIN SET