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

BAYER RAPIDLAB 1200 SYSTEM

K Number: K031560 · Decision Dec 17, 2003
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
186
Applicant Total
41
Review Days
212

Basic Information

Device Name
BAYER RAPIDLAB 1200 SYSTEM
K Number
K031560
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BAYER HEALTHCARE, LLC
Date Received
May 19, 2003
Decision Date
December 17, 2003
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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