510(k) Report

510(k) · Cleared

Cleared

GEM Premier 5000

K173403510(k) TraditionalCleared Dec 29, 201759-day reviewClass II21 CFR 862.1120

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

Instrumentation Laboratory CO · CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

Cleared on Dec 29, 2017 as substantially equivalent to K133407 (Instrumentation Laboratory CO, 2014) after a 59-day review. Its family tree reaches back 9 generations to 1980. 2 later devices descend from it.

Decided
Dec 29, 2017
Review
59 days
Class
Class II
Product code
CHL
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K801848 (1980). 24 ancestors in all, the oldest K790608 (1979). 2 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK801848 ICA1 Ionized Calcium AnalyzerThe London Co. · 1980
  2. 5 generations between
  3. 3 generations backK093623 Gem Premier 4000 with Iqm (Addition of Total Bilirubin Parameter)…Instrumentation Laboratory CO · 2010 · Recalled
  4. 2 generations backK112995 Gem Premier 4000Instrumentation Laboratory CO · 2012
  5. 1 generation backK133407 Gem Premier 4000Instrumentation Laboratory CO · 2014
  6. This deviceK173403 GEM Premier 5000Instrumentation Laboratory CO · 2017
  7. Descendant · cites it directly · 1 of its ownK203790 GEM Premier 5000Instrumentation Laboratory CO · 2021 · Recalled
  8. Descendant · 2 generations on · 0 of its ownK223608 GEM Premier 7000 with IQM3Instrumentation Laboratory Company · 2023 · Recalled
Show all 9 generations
  1. Root · 9 generations backK801848 ICA1 Ionized Calcium AnalyzerThe London Co. · 1980
  2. 8 generations backK963800 IL SynthesisInstrumentation Laboratory CO · 1996
  3. 7 generations backK992834 Gem Premier 3000Instrumentation Laboratory CO · 1999 · Recalled
  4. 6 generations backK022158 Iqm (Intelligent Quality Management) on the Gem Premier 3000, CVP…Instrumentation Laboratory CO · 2002
  5. 5 generations backK052121 Gem Premier 3000Instrumentation Laboratory CO · 2005 · Recalled
  6. 4 generations backK061974 Gem Premier 4000 with Iqm, Model 4000; Gem CVP 1 and 2 with CO-OX…Instrumentation Laboratory CO · 2006 · Recalled
  7. 3 generations backK093623 Gem Premier 4000 with Iqm (Addition of Total Bilirubin Parameter)…Instrumentation Laboratory CO · 2010 · Recalled
  8. 2 generations backK112995 Gem Premier 4000Instrumentation Laboratory CO · 2012
  9. 1 generation backK133407 Gem Premier 4000Instrumentation Laboratory CO · 2014
  10. This deviceK173403 GEM Premier 5000Instrumentation Laboratory CO · 2017

Most influential descendants

Showing 2 of 2 · See all
  • K203790GEM Premier 5000Instrumentation Laboratory CO · 2021 · cites it directly1descendant
  • K223608GEM Premier 7000 with IQM3Instrumentation Laboratory Company · 2023 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K801848ICA1 Ionized Calcium AnalyzerThe London Co.1980—
−8K963800IL SynthesisInstrumentation Laboratory CO1996—
−7K992834Gem Premier 3000Instrumentation Laboratory CO19995
−6K022158Iqm (Intelligent Quality Management) on the Gem Premier 3000, CVP (Calibration…Instrumentation Laboratory CO2002—
−5K052121Gem Premier 3000Instrumentation Laboratory CO20052
−4K061974Gem Premier 4000 with Iqm, Model 4000; Gem CVP 1 and 2 with CO-OX; Gem CVP 3…Instrumentation Laboratory CO20064
−3K093623Gem Premier 4000 with Iqm (Addition of Total Bilirubin Parameter), Gem CVP 2…Instrumentation Laboratory CO20105
−2K112995Gem Premier 4000Instrumentation Laboratory CO2012—
−1K133407Gem Premier 4000Instrumentation Laboratory CO2014—
0 (this device)K173403GEM Premier 5000Instrumentation Laboratory CO2017—
+1K203790GEM Premier 5000Instrumentation Laboratory CO202125
+2K223608GEM Premier 7000 with IQM3Instrumentation Laboratory Company20232

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198410
198610
198910
199220
199410
199520
199620
199710
199810
199910
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202310
FIG. 1 — Lineage of K173403, 1980–2023Source: 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
Get a 510(k) Report

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
*K133407Gem Premier 4000
Summary page 9
…GEM Premier 4000 GEM Premier 5000 510(k) No. K133407 Pending Manufacturer Instrumentation…
Instrumentation Laboratory CO2014—

Also cleared against K133407: 6 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K203790GEM Premier 5000Instrumentation Laboratory CO20211

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

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 37 years and passes through 2 companies; a new generation was cleared every 3.0 years on median.
  • 9 of the 24 ancestors have a recall of any class.
  • Of its descendants, K203790 (Instrumentation Laboratory CO, 2021) has gone furthest, with 1 descendant of its own.
  • 6 other devices also cite its predicate K133407.

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. 2017, 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 GEM Premier 5000 is a portable critical care system for use by health care professionals to rapidly analyze heparinized whole blood samples at the point of health care delivery in a clinical setting and in a central laboratory. The instrument provides quantitative measurements of pH, pCO2, pO2, sodium, potassium, chloride, ionized calcium, glucose, lactate, hematocrit, total bilirubin and CO-Oximetry (tHb, O2Hb, COHb, MetHb, HHb, sO2*) parameters…

Read the full statement (522 words)

The GEM Premier 5000 is a portable critical care system for use by health care professionals to rapidly analyze heparinized whole blood samples at the point of health care delivery in a clinical setting and in a central laboratory. The instrument provides quantitative measurements of pH, pCO2, pO2, sodium, potassium, chloride, ionized calcium, glucose, lactate, hematocrit, total bilirubin and CO-Oximetry (tHb, O2Hb, COHb, MetHb, HHb, sO2*) parameters from arterial, venous or capillary heparinized whole blood. These parameters, along with derived parameters, aid in the diagnosis of a patient’s acid/base status, electrolyte and metabolite balance and oxygen delivery capacity.

*sO2 = ratio between the concentration of oxyhemoglobin and oxyhemoglobin plus deoxyhemoglobin.

* pH, pCO2, and pO2 measurements in whole blood are used in the diagnosis and treatment of life-threatening acid-base disturbances.

* Electrolytes in the human body have multiple roles. Nearly all metabolic processes depend on or vary with electrolytes:

* Sodium (Na+) 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.

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

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

* Chloride (Cl-) measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders, such as cystic fibrosis and diabetic acidosis.

* Hematocrit (Hct) measurements in whole blood of the packed red cell volume of a blood sample are used to distinguish normal from abnormal states, such as anemia and erythrocytosis (an increase in the number of red cells).

* Glucose (Glu) measurement is used in the diagnosis, monitoring and treatment of carbohydrate metabolism disturbances including diabetes mellitus, neonatal hypoglycemia, idiopathic hypoglycemia, and pancreatic islet cell carcinoma.

* Lactate (Lac) measurement is used:

* to evaluate the acid-base status of patients suspected of having lactic acidosis;

* to monitor tissue hypoxia and strenuous physical exertion;

* in the diagnosis of hyperlactatemia.

« Total Bilirubin (tBili) measurement is used to aid in assessing the risk of kernicterus and hyperbilirubinemia in neonates.

* CO-Oximetry (tHb, COHb, MetHb, O2Hb, HHb, and sO2) evaluates the ability of the blood to carry oxygen by measuring total hemoglobin and determining the percentage of functional and dysfunctional hemoglobin species.

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

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

* MetHb: Methemoglobin measurements are used to determine different conditions of methemoglobinemia.

* HHb: Deoxyhemoglobin, as a fraction of total hemoglobin, is used in combination with oxyhemoglobin to measure oxygen status.

* O2Hb: Oxyhemoglobin, as a fraction of total hemoglobin, is used in combination with deoxyhemoglobin to measure oxygen status.

» 5O2: Oxygen saturation, more specifically the ratio between the concentration of oxyhemoglobin and oxyhemoglobin plus deoxyhemoglobin, is used to measure oxygen status.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K173403: GEM Premier 5000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173403

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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