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

MULTECON BLOOD GAS CONTROL

K Number: K790813 · Decision Jun 28, 1979
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
66
Applicant Total
24
Review Days
62

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Basic Information

Device Name
MULTECON BLOOD GAS CONTROL
K Number
K790813
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Ortho Diagnostics, Inc.
Date Received
April 27, 1979
Decision Date
June 28, 1979
Product Code
JJS
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
JJS Controls For Blood-Gases, (Assayed And Unassayed)

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K Number Device Name
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K800357 BI-LEVEL ASSAYED CARD. DRUG CONT., I,II
K800310 ORTHO ANTISERA CONTROL
K791791 ORTHO ANTIBODY ENHANCEMENT SOLUTION
K791301 ORTHO TSH RIA KIT
K782063 PREGNANCY, SENSIDEX TUBE TEST
K782166 SLIDE TEST FOR PREGNANCY, GRAVINDEX 90
K781638 RUBINDEX*DIRECT SYSTEM
K781860 ASSAY, CHROMOGENIC ANTITHROMBIN III
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