510(k) Report

510(k) · Cleared

Recalled · Class II · 2012

ABL90

K111897510(k) SpecialCleared Jul 19, 201114-day reviewClass II21 CFR 862.1120Recalls 2

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Radiometer Medical Aps · CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

Cleared on Jul 19, 2011 as substantially equivalent to K092686 (Radiometer Medical Aps, 2010) after a 14-day review. Its family tree reaches back 7 generations to 1986. 1 later device descends from it. It has been recalled 2 times.

Decided
Jul 19, 2011
Review
14 days
Class
Class II
Product code
CHL
Recalls
2
Predicates
1

Its longest line of descent runs back 7 generations to K861087 (1986). 19 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1999: 1 other ancestor1998: 2 other ancestors1996: 3 other ancestors1997: 1 other ancestor1995: 1 other ancestor1992: 1 other ancestor1987: 1 other ancestor1986: 1 other ancestor2013: 1 descendant clearedK861087 · Avl Model 983 Electrolyte Analyzer · Avl Scientific Corp. · 1986K961458 · Avl 9180 Electrolyte Analyzer · Avl Scientific Corp. · 1996 · recalledK972673 · Avl 9181 Electrolyte Analyzer · Avl Scientific Corp. · 1997 · recalledK992859 · ABL700 Series Analyzer with Autocheck Module · Radiometer America, Inc. · 2000 · recalledK041874 · ABL800 Flex · Radiometer Medical Aps · 2004 · recalledK050869 · Modification to ABL800 Flex · Radiometer Medical Aps · 2005 · recalledK092686 · ABL90 Flex Series · Radiometer Medical Aps · 2010 · recalled1990200020102020
  1. Root · 7 generations backK861087 Avl Model 983 Electrolyte AnalyzerAvl Scientific Corp. · 1986
  2. 6 generations backK961458 Avl 9180 Electrolyte AnalyzerAvl Scientific Corp. · 1996 · Recalled
  3. 5 generations backK972673 Avl 9181 Electrolyte AnalyzerAvl Scientific Corp. · 1997 · Recalled
  4. 4 generations backK992859 ABL700 Series Analyzer with Autocheck ModuleRadiometer America, Inc. · 2000 · Recalled
  5. 3 generations backK041874 ABL800 FlexRadiometer Medical Aps · 2004 · Recalled
  6. 2 generations backK050869 Modification to ABL800 FlexRadiometer Medical Aps · 2005 · Recalled
  7. 1 generation backK092686 ABL90 Flex SeriesRadiometer Medical Aps · 2010 · Recalled
  8. This deviceK111897 ABL90Radiometer Medical Aps · 2011
  9. Descendant · cites it directly · 0 of its ownK123748 ABL90 FlexRadiometer Medical Aps · 2013

Most influential descendants

Showing 1 of 1 · See all
  • K123748ABL90 FlexRadiometer Medical Aps · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K861087Avl Model 983 Electrolyte AnalyzerAvl Scientific Corp.1986—
−6K961458Avl 9180 Electrolyte AnalyzerAvl Scientific Corp.19961
−5K972673Avl 9181 Electrolyte AnalyzerAvl Scientific Corp.19977
−4K992859ABL700 Series Analyzer with Autocheck ModuleRadiometer America, Inc.20004
−3K041874ABL800 FlexRadiometer Medical Aps200422
−2K050869Modification to ABL800 FlexRadiometer Medical Aps20051
−1K092686ABL90 Flex SeriesRadiometer Medical Aps201010
0 (this device)K111897ABL90Radiometer Medical Aps2011—
+1K123748ABL90 FlexRadiometer Medical Aps2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198710
199210
199510
199630
199710
199820
199910
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
FIG. 1 — Lineage of K111897, 1986–2013Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in CHL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new CHL device

  1. #1 K252207 ABL90 FLEX PLUS System, safeCLINITUBESscore 14.1 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K092686ABL90 Flex Series
Summary page 1
…ption is substantially equivalent in Intended Use, fundamental scientific technology, features, and characteristics to the predicate: 510(k) Number/Device Manufacturer: K092686 ABL90 Flex, Radiometer Medical ApS Section 5 Page 2 PaQe 1 of 2 Special…
Radiometer Medical Aps201010

Also cleared against K092686: 5 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K123748ABL90 FlexRadiometer Medical Aps20130

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Jul 5, 2012Class IIZ-2163-2012Software designA customer has reported an error on an ABL8xx configured to a Hospital Information System using the data transfer protocol HL7 version 2.5. If the instrument transmits results to a HIS system and the connection is broken the results are…
Jul 5, 2012Class IIZ-2162-2012Software designA customer has reported an error on an ABL8xx configured to a Hospital Information System using the data transfer protocol HL7 version 2.5. If the instrument transmits results to a HIS system and the connection is broken the results are…

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 25 years and passes through 3 companies; a new generation was cleared every 2.4 years on median.
  • 12 of the 19 ancestors have a recall of any class.
  • Of its descendants, K123748 (Radiometer Medical Aps, 2013) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K092686.

How does its category compare?

All CHL devices

CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · CHL

1in 2025

2007: 12008: 12010: 12011: 42012: 42013: 52014: 32015: 42016: 32017: 12018: 12020: 42021: 22023: 52024: 12025: 12026 (partial year): 1
2007high 5 (2013) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CHL

267in 2023

2011: 108 days median2012: 65 days median2013: 152 days median2014: 68 days median2015: 155 days median2016: 306 days median2020: 100 days median2023: 267 days median
2007high 306 (2016) · low 65 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · CHL

13so far in 2026, the most since 2007

2007: 62008: 52009: 62010: 72011: 12012: 92013: 12014: 12015: 32016: 12017: 12018: 32020: 22023: 42024: 92026 (partial year): 13
2007high 13 (2026) · low 0 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · CHL

210in 2025

2007: 162008: 402009: 742010: 202011: 502012: 642013: 622014: 932015: 552016: 1182017: 2062018: 1742019: 1412020: 1172021: 1472022: 1382023: 1772024: 1962025: 210
2007high 210 (2025) · low 16 (2007)2025

MAUDE reports naming product code CHL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—616
20081—540
20090—674
20101—720
20114108150
2012465964
20135152162
2014368193
20154155355
201633061118
20171—1206
20181—3174
20190—0141
202041002117
20212—0147
20220—0138
202352674177
20241—9196
20251—0210
20261—13—

What is it indicated for?

The ABL90 FLEX is a portable, automated analyzer that measures pH, blood gases, electrolytes, glucose, lactate and oximetry in heparinized whole blood. The ABL9O FLEX is intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting. These tests are only performed under a physician's order: pH, p0 2 and pCO2 : pH, pCO2 and p0 2 measurements are used…

Read the full statement (352 words)

The ABL90 FLEX is a portable, automated analyzer that measures pH, blood gases, electrolytes, glucose, lactate and oximetry in heparinized whole blood. The ABL9O FLEX is intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting.

These tests are only performed under a physician's order:

pH, p0 2 and pCO2 : pH, pCO2 and p0 2 measurements are used in the diagnosis and treatment of life-threatening acid-base disturbances.

Potassium (cK+): potassium measurements are used to monitor electrolyte balance in the diagnosis and treatment of disease conditions characterized by low or high blood potassium levels.

Sodium (cNa±): sodium measurements are used in the diagnosis and treatment of aldosteronism, diabetes insipidus, adrenal hypertension, Addison's disease, dehydration, inappropriate antidiuretic secretion, or other diseases involving electrolyte imbalance.

Calcium (cCa2+): calcium measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany.

Chloride (cCl-): chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such a cystic fibrosis and diabetic acidosis.

Glucose (cGlu): glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.

Lactate (cLac): The lactate measurements measure the concentration of lactate in plasma. Lactate measurements are used to evaluate the acid-base status and are used in the diagnosis and treatment of lactic acidosis (abnormally high acidity of the blood.)

Total Hemoglobin (ctHb): total hemoglobin measurements are used to measure the hemoglobin content of whole blood for the detection of anemia.

s02: oxygen saturation, more specifically the ratio between the concentration of oxyhemoglobin and oxyhemoglobin plus reduced hemoglobin.

FO2Hb: oxyhemoglobin as a fraction of total hemoglobin.

FCOHb: carboxyhemoglobin measurements are used to determine the carboxyhemoglobin content of human blood as an aid in the diagnosis of carbon monoxide poisoning.

FMetHb: methemoglobin as a fraction of total hemoglobin.

FHHb: reduced hemoglobin as a fraction of total hemoglobin.

Fraction of Fetal Hemoglobin (FHbF): FHbF indicates the amount of fetal hemoglobin. FHbF is seldom used clinically.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111897: ABL90.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K111897

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026