Cleared Traditional

K131988 - ABL90 FLEX ANALYZER

K131988 is an FDA 510(k) clearance for ABL90 FLEX ANALYZER, manufactured by Radiometer Medical Aps. The device is a Class 2 Chemistry device with product code CHL cleared through the Traditional 510(k) pathway after a 81-day FDA review.

K131988 · Radiometer Medical Aps · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2013
Decision
81d
Days
Class 2
Risk

K131988 is an FDA 510(k) clearance for the ABL90 FLEX ANALYZER. Classified as Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph (product code CHL), Class II - Special Controls.

Submitted by Radiometer Medical Aps (Bronshoj, DK). The FDA issued a Cleared decision on September 17, 2013 after a review of 81 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1120 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Radiometer Medical Aps devices

FDA 510(k) Submission Details - K131988

510(k) Number K131988 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 28, 2013
Decision Date September 17, 2013
Days to Decision 81 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
7d faster than avg
Panel avg: 88d · This submission: 81d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CHL Device Classification - Class 2, Special Controls

Product Code CHL Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1120
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CHL Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph

All 151
Devices cleared under the same product code (CHL) and FDA review panel - the closest regulatory comparables to K131988.
Stat Profile Prime ABG Analyzer System (incl. Controls, Calibrators)
K142220 · Nova Biomedical Corporation · Oct 2014
NOVA STAT PROFILE PRIME CCS ANALYZER SYSTEM
K131703 · Nova Biomedical Corporation · Mar 2014
GEM PREMIER 4000
K133407 · Instrumentation Laboratory CO · Jan 2014
ABL90 FLEX
K130144 · Radiometer Medical Aps · Jul 2013
ABL90 FLEX
K123748 · Radiometer Medical Aps · May 2013
MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM
K122539 · Siemens Healthcare Diagnostics · Apr 2013