510(k) Report

510(k) · Cleared

Cleared

G+ System

K113853510(k) TraditionalCleared May 8, 2012131-day reviewClass II21 CFR 868.1890

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

Glytec, LLC · NDC Calculator, Drug Dose

Cleared on May 8, 2012 as substantially equivalent to K101344 (Glytec, LLC (Formally Known AS Glucotec, Inc.), 2010) after a 131-day review. Its family tree reaches back 8 generations to 1994. 1 of the 45 devices in its family, counting itself, has a Class I recall. 12 later devices descend from it.

Decided
May 8, 2012
Review
131 days
Class
Class II
Product code
NDC
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K941811 (1994). 32 ancestors in all, the oldest K822695 (1982). 12 later devices descend from it, 5 citing it directly. 1 of the 45 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2005: 2 other ancestors2004: 3 other ancestors, 1 with a Class I recall11998: 1 other ancestor2002: 2 other ancestors1992: 3 other ancestors2001: 1 other ancestor2000: 1 other ancestor1999: 4 other ancestors1997: 2 other ancestors1993: 1 other ancestor1982: 1 other ancestor1996: 1 other ancestor1995: 1 other ancestor1994: 1 other ancestor2017: 2 descendants cleared2014: 2 descendants cleared2015: 1 descendant cleared2020: 2 descendants cleared2018: 1 descendant cleared2026: 2 descendants cleared2021: 1 descendant cleared2024: 1 descendant clearedK941811 · HP M1175A, M1176A, Component Monitoring System · Hewlett-Packard Co. · 1994K960934 · HP M1205A Omnicare Component Monitor System Model 24 · Hewlett-Packard Co. · 1996×2: 2 generations cleared close together, K981376 (1999), K990125 (1999) K992636 · HP Carevue 9000 Clinical Information System, Model M2331A · Hewlett-Packard Co. · 1999 · recalledK023674 · Philips Drug Calculator Software · Philips Medical Systems · 2002K061110 · Glucommander Plus · Collaborativemed, LLC · 2006K101344 · G+ System · Glytec, LLC (Formally Known AS Glucotec, Inc.) · 201019801990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 5 other ancestors, 1 with a Class I recall14 generations back: 4 other ancestors5 generations back: 9 other ancestors6 generations back: 2 other ancestors7 generations back: 4 other ancestors 1 generation forward: 5 descendants2 generations forward: 3 descendants3 generations forward: 2 descendants4 generations forward: 1 descendant5 generations forward: 1 descendant K101344 · G+ System · Glytec, LLC (Formally Known AS Glucotec, Inc.) · 2010K061110 · Glucommander Plus · Collaborativemed, LLC · 2006K023674 · Philips Drug Calculator Software · Philips Medical Systems · 2002K992636 · HP Carevue 9000 Clinical Information System, Model M2331A · Hewlett-Packard Co. · 1999 · recalledK990125 · HP Viridia Component Monitoring System, Model Rev. K · Hewlett-Packard GmbH · 1999K981376 · Hewlett-Packard M1205A Viridia 24 CT · Hewlett-Packard Co. · 1999K960934 · HP M1205A Omnicare Component Monitor System Model 24 · Hewlett-Packard Co. · 1996K941811 · HP M1175A, M1176A, Component Monitoring System · Hewlett-Packard Co. · 1994−50+5
  1. Root · 8 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 7 generations backK960934 HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co. · 1996
  3. 6 generations backK981376 Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co. · 1999
  4. 5 generations backK990125 HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH · 1999
  5. 4 generations backK992636 HP Carevue 9000 Clinical Information System, Model M2331AHewlett-Packard Co. · 1999 · Recalled
  6. 3 generations backK023674 Philips Drug Calculator SoftwarePhilips Medical Systems · 2002
  7. 2 generations backK061110 Glucommander PlusCollaborativemed, LLC · 2006
  8. 1 generation backK101344 G+ SystemGlytec, LLC (Formally Known AS Glucotec, Inc.) · 2010
  9. This deviceK113853 G+ SystemGlytec, LLC · 2012
  10. Descendant · cites it directly · 8 of its ownK132547 Endo Tool Glucose Management System (Egms)Monarch Medical Technologies · 2014 · Recalled
  11. Descendant · 2 generations on · 3 of its ownK200443 EndoTool IV 1.10Monarch Medical Technologies, LLC · 2020
  12. Descendant · 3 generations on · 2 of its ownK201619 EndoTool IV SystemMonarch Medical Technologies, LLC · 2020
  13. Descendant · cites it directly · 2 of its ownK142918 EndoTool SubQMonarch Medical Technologies · 2015
  14. Descendant · 4 generations on · 1 of its ownK241088 EndoTool IV (3.1)Monarch Medical Technologies · 2024

Showing 5 of 12 descendants. See all descendants

Descendants cleared per year

2014: 22015: 12017: 22018: 12020: 22021: 12024: 12026: 2
2014high 2 (2014) · low 0 (2016)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 12 · See all
  • K132547Endo Tool Glucose Management System (Egms)Monarch Medical Technologies · 2014 · cites it directly8descendants
  • K200443EndoTool IV 1.10Monarch Medical Technologies, LLC · 2020 · 2 generations on3descendants
  • K201619EndoTool IV SystemMonarch Medical Technologies, LLC · 2020 · 3 generations on2descendants
  • K142918EndoTool SubQMonarch Medical Technologies · 2015 · cites it directly2descendants
  • K241088EndoTool IV (3.1)Monarch Medical Technologies · 2024 · 4 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K941811HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co.1994—
−7K960934HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co.1996—
−6K981376Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co.1999—
−5K990125HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH1999—
−4K992636HP Carevue 9000 Clinical Information System, Model M2331AHewlett-Packard Co.19998
−3K023674Philips Drug Calculator SoftwarePhilips Medical Systems2002—
−2K061110Glucommander PlusCollaborativemed, LLC2006—
−1K101344G+ SystemGlytec, LLC (Formally Known AS Glucotec, Inc.)2010—
0 (this device)K113853G+ SystemGlytec, LLC2012—
+1K132547Endo Tool Glucose Management System (Egms)Monarch Medical Technologies20141
+2K200443EndoTool IV 1.10Monarch Medical Technologies, LLC2020—
+3K201619EndoTool IV SystemMonarch Medical Technologies, LLC2020—
+1K142918EndoTool SubQMonarch Medical Technologies2015—
+4K241088EndoTool IV (3.1)Monarch Medical Technologies2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199230
199310
199410
199510
199610
199720
199810
199940
200010
200110
200220
200431
200520

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201420
201510
201720
201810
202020
202110
202410
202620
FIG. 1 — Lineage of K113853, 1994–2026Source: 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.

1 device in this family has a Class I recall. 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 NDC device

  1. #1 K242775 InPen System App (MMT-8060 (iOS), MMT-8061…score 18.0 · 10 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
*K101344G+ System
Summary page 2
…ection 3 510(k) Summary of Safety and Effectiveness April 30, 2012 GlyTec, LLC G+ System - #K1 01 344 (6/26/20 10) Device Description The Glytec, LILC Glucommander System is a software device used to evaluate current and cumulati…
Glytec, LLC (Formally Known AS Glucotec, Inc.)2010—

What descends from it? (12)

See all 12

5 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K132547Endo Tool Glucose Management System (Egms)Monarch Medical Technologies20148
K142918EndoTool SubQMonarch Medical Technologies20152
K152300GlucommanderGlytec, LLC20171
K160673Insulin Algorithms SystemInsulin Algorithms20170
K141321Glucostabilizer Insulin Dosing CalculatorMedical Decision Network20140

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K042873Animas Model IR1250 Insulin Infusion PumpAnimas Corp. · 2004 · 3 generations back · ◆ in the 2004 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 18 years and passes through 6 companies; a new generation was cleared every 2.6 years on median.
  • 6 of the 32 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K132547 (Monarch Medical Technologies, 2014) has gone furthest, with 8 descendants of its own.

How does its category compare?

All NDC devices

NDC Calculator, Drug Dose: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · NDC

2in 2025

2007: 12008: 22010: 12012: 22014: 32015: 32016: 22017: 82018: 32019: 12020: 52021: 32023: 32024: 32025: 22026 (partial year): 4
2007high 8 (2017) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NDC

60in 2024

2014: 118 days median2015: 199 days median2017: 189 days median2018: 220 days median2020: 53 days median2021: 269 days median2023: 126 days median2024: 60 days median2026 (partial year): 90 days median
2007high 269 (2021) · low 53 (2020)2026

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

Recalls per year · NDC

1in 2025

2016: 12017: 22018: 12019: 12022: 12025: 12026 (partial year): 2
2007high 2 (2017) · low 0 (2007)2026

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

Adverse event reports per year · NDC

299in 2025

2008: 72009: 42010: 182011: 112012: 22013: 12014: 12015: 12016: 182017: 252018: 212019: 182020: 102021: 112022: 3472023: 4632024: 1682025: 299
2007high 463 (2023) · low 0 (2007)2025

MAUDE reports naming product code NDC, 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—00
20082—07
20090—04
20101—018
20110—011
20122—02
20130—01
2014311801
2015319901
20162—118
20178189225
20183220121
20191—118
2020553010
20213269011
20220—1347
202331260463
20243600168
20252—1299
20264902—

What is it indicated for?

The Glucommander System is a glycemic management tool intended to evaluate current and cumulative patient blood glucose values and coupled with patient information including age, weight and height, and, based on the aggregate of these measurement parameters, whether one or many, recommend an IV dosage of insulin, glucose or saline or a subcutaneous basal and bolus insulin dosing recommendation to adjust and maintain the blood glucose level towards a…

Read the full statement (161 words)

The Glucommander System is a glycemic management tool intended to evaluate current and cumulative patient blood glucose values and coupled with patient information including age, weight and height, and, based on the aggregate of these measurement parameters, whether one or many, recommend an IV dosage of insulin, glucose or saline or a subcutaneous basal and bolus insulin dosing recommendation to adjust and maintain the blood glucose level towards a configurable clinician determined target range. The Glucommander System is indicated for use in adult and pediatric (ages 2 - 17 years) patients.

The Glucommander System logic is not a substitute for, but rather an adjunct to clinical reasoning. The measurements and calculations generated are intended to be used by qualified and trained medical personnel in evaluating patient conditions in conjunction with clinical history, symptoms, and other diagnostic measurements, as well as the medical professional's clinical judgment. No medical decision should be based solely on the recommended guidance provided by this software program.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K113853: G+ System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113853

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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