510(k) K000520

Device
C-IT
Applicant
BREGAS AB
510(k) number
K000520
Product code
CCK  
Decision
Substantially Equivalent (SESE)
Decision date
2000-05-16
Date received
2000-02-16
Regulation
868.1400
Classification name
Analyzer, Gas, Carbon-dioxide, Gaseous-phase
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Related Records

Applicant Contact

Contact
PAUL KRILL
Address
Ulvsundavagen 178b Bromma SE SE-16867 SE-16867

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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Legacy Summary

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FDA Review

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