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

FLUSH SOLUTION CONCENTRATE-BLOOD GAS

K Number: K840300 · Decision Mar 23, 1984
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
49
Review Days
59

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Basic Information

Device Name
FLUSH SOLUTION CONCENTRATE-BLOOD GAS
K Number
K840300
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bionostics, Inc.
Date Received
January 24, 1984
Decision Date
March 23, 1984
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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K101831 ENTERIX INSUREFIT FOB CONTROLS, MODEL 16800
K091914 OMNIS HEALTH EMBRACE GLUCOSE CONTROL SOLUTION
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