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

DU PONT ISE SENSOR CARTRIDGE/REVISED TCO2 ELECTROD

K Number: K932044 · Decision Jul 27, 1993
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
88
Applicant Total
28
Review Days
91

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Basic Information

Device Name
DU PONT ISE SENSOR CARTRIDGE/REVISED TCO2 ELECTROD
K Number
K932044
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1600
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dupont Medical Products
Date Received
April 27, 1993
Decision Date
July 27, 1993
Product Code
CEM
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
CEM Electrode, Ion Specific, Potassium

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K941050 DUPONT ACA STAR
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K941146 DUPONT ACA PLUS THYROID STIMULATING HORMONE SYSTEM
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