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

DIAGNOSTICS PO 2 ELECTROLYTE

K Number: K831013 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
89
Review Days
70

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Basic Information

Device Name
DIAGNOSTICS PO 2 ELECTROLYTE
K Number
K831013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Fisher Scientific Co., LLC
Date Received
March 30, 1983
Decision Date
June 8, 1983
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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