FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

ABL90 FLEX PLUS System, safeCLINITUBES

K Number: K252207 · Decision Apr 10, 2026
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
5
Review Days
270

Basic Information

Device Name
ABL90 FLEX PLUS System, safeCLINITUBES
K Number
K252207
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radiometer Medicals Aps
Date Received
July 14, 2025
Decision Date
April 10, 2026
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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Other Clearances by Radiometer Medicals Aps

K Number Device Name
K252475 ABL90 FLEX PLUS System
K252488 ABL90 FLEX PLUS System
K241037 ABL90 FLEX PLUS System
K240998 ABL90 FLEX PLUS System