510(k) Report

510(k) · Cleared

Cleared

Gal-1A Blood Glucose Monitoring System

K113208510(k) SpecialCleared Jan 26, 201286-day reviewClass II21 CFR 862.1345

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

Apex BioTechnology Corp. · CGA Glucose Oxidase, Glucose

Cleared on Jan 26, 2012 as substantially equivalent to K102816 (Apex BioTechnology Corp., 2011) after an 86-day review. Its family tree reaches back 4 generations to 2001. 9 later devices descend from it.

Decided
Jan 26, 2012
Review
86 days
Class
Class II
Product code
CGA
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K011233 (2001). 5 ancestors in all. 9 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2014: 1 descendant cleared2022: 3 descendants cleared2015: 1 descendant cleared2016: 1 descendant cleared2017: 1 descendant cleared2018: 1 descendant cleared2021: 1 descendant clearedK011233 · Modification to Glucosure BGM System, Model 221100 · Apex BioTechnology Corp. · 2001 · recalledK062799 · Gluco Track Blood Glucose Monitoring System · Apex BioTechnology Corp. · 2007K073648 · Glucosure Star Blood Glucose Monitoring System, Model AS90000E1 · Apex BioTechnology Corp. · 2008K102816 · Gal-1C Blood Glucose Monitoring System, Gal-1C Test Strips · Apex BioTechnology Corp. · 2011200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 2 descendants3 generations forward: 3 descendants4 generations forward: 1 descendant K102816 · Gal-1C Blood Glucose Monitoring System, Gal-1C Test Strips · Apex BioTechnology Corp. · 2011K073648 · Glucosure Star Blood Glucose Monitoring System, Model AS90000E1 · Apex BioTechnology Corp. · 2008K062799 · Gluco Track Blood Glucose Monitoring System · Apex BioTechnology Corp. · 2007K011233 · Modification to Glucosure BGM System, Model 221100 · Apex BioTechnology Corp. · 2001 · recalled0
  1. Root · 4 generations backK011233 Modification to Glucosure BGM System, Model 221100Apex BioTechnology Corp. · 2001 · Recalled
  2. 3 generations backK062799 Gluco Track Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2007
  3. 2 generations backK073648 Glucosure Star Blood Glucose Monitoring System, Model AS90000E1Apex BioTechnology Corp. · 2008
  4. 1 generation backK102816 Gal-1C Blood Glucose Monitoring System, Gal-1C Test StripsApex BioTechnology Corp. · 2011
  5. This deviceK113208 Gal-1A Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2012
  6. Descendant · cites it directly · 3 of its ownK141036 BGM009 Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2015
  7. Descendant · cites it directly · 3 of its ownK131750 Autosure HT Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2014
  8. Descendant · 2 generations on · 2 of its ownK170267 BGM009 Plus Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2017
  9. Descendant · 2 generations on · 2 of its ownK161299 BGM014 Blood Glucose Monitoring System, BGM014 Pro Blood Glucose…Apex BioTechnology Corp. · 2016
  10. Descendant · 3 generations on · 1 of its ownK202885 GlucoSure HT Plus Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2021

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

2014: 12015: 12016: 12017: 12018: 12021: 12022: 3
2014high 3 (2022) · low 0 (2019)2026

Most influential descendants

Showing 5 of 9 · See all
  • K141036BGM009 Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2015 · cites it directly3descendants
  • K131750Autosure HT Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2014 · cites it directly3descendants
  • K170267BGM009 Plus Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2017 · 2 generations on2descendants
  • K161299BGM014 Blood Glucose Monitoring System, BGM014 Pro Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2016 · 2 generations on2descendants
  • K202885GlucoSure HT Plus Blood Glucose Monitoring SystemApex BioTechnology Corp. · 2021 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K011233Modification to Glucosure BGM System, Model 221100Apex BioTechnology Corp.20011
−3K062799Gluco Track Blood Glucose Monitoring SystemApex BioTechnology Corp.2007—
−2K073648Glucosure Star Blood Glucose Monitoring System, Model AS90000E1Apex BioTechnology Corp.2008—
−1K102816Gal-1C Blood Glucose Monitoring System, Gal-1C Test StripsApex BioTechnology Corp.2011—
0 (this device)K113208Gal-1A Blood Glucose Monitoring SystemApex BioTechnology Corp.2012—
+1K141036BGM009 Blood Glucose Monitoring SystemApex BioTechnology Corp.2015—
+1K131750Autosure HT Blood Glucose Monitoring SystemApex BioTechnology Corp.2014—
+2K170267BGM009 Plus Blood Glucose Monitoring SystemApex BioTechnology Corp.2017—
+2K161299BGM014 Blood Glucose Monitoring System, BGM014 Pro Blood Glucose Monitoring…Apex BioTechnology Corp.2016—
+3K202885GlucoSure HT Plus Blood Glucose Monitoring SystemApex BioTechnology Corp.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201510
201610
201710
201810
202110
202230
FIG. 1 — Lineage of K113208, 2001–2022Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 CGA? 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 CGA device

  1. #1 K252488 ABL90 FLEX PLUS Systemscore 12.8 · 6 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
*K102816Gal-1C Blood Glucose Monitoring System, Gal-1C Test Strips
Summary page 1
…tion: Glucose test system, 21 CFR 862.1345, Class 11 Product Codes: CGA, NBW Predicate Device: GAL-IC Blood Glucose Monitoring System (k102816) GAL-IC Blood Glucose Test Strip (k102816) Device Description: The GAL-lA blood glucose meter…
Apex BioTechnology Corp.2011—

Also cleared against K102816: 1 other device →

What descends from it? (9)

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

NumberDeviceApplicantDecidedDescendants
K141036BGM009 Blood Glucose Monitoring SystemApex BioTechnology Corp.20153
K131750Autosure HT Blood Glucose Monitoring SystemApex BioTechnology Corp.20143
K213887GAL-1A Plus Blood Glucose Monitoring SystemApex BioTechnology Corp.20220

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 11 years and passes through 1 company; a new generation was cleared every 3.4 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K141036 (Apex BioTechnology Corp., 2015) has gone furthest, with 3 descendants of its own.
  • 1 other device also cites its predicate K102816.

How does its category compare?

All CGA devices

CGA Glucose Oxidase, Glucose: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · CGA

2in 2024

2007: 72008: 62009: 102010: 82011: 92012: 102013: 32014: 52015: 42016: 42017: 22018: 22019: 22020: 22021: 12022: 12023: 42024: 22026 (partial year): 1
2007high 10 (2009) · low 0 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CGA

249in 2023

2007: 122 days median2008: 56 days median2009: 155 days median2010: 122 days median2011: 217 days median2012: 123 days median2013: 441 days median2014: 265 days median2015: 150 days median2016: 157 days median2023: 249 days median
2007high 441 (2013) · low 56 (2008)2026

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

Recalls per year · CGA

3in 2023

2007: 22008: 22009: 42010: 62011: 32013: 32014: 22015: 6, 2 Class I2016: 22019: 12023: 3
2007high 6 (2010) · low 0 (2012)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · CGA

59in 2025

2007: 292008: 372009: 752010: 1722011: 4232012: 2332013: 1722014: 1222015: 1552016: 362017: 922018: 692019: 1162020: 682021: 482022: 2722023: 1,1412024: 2662025: 59
2007high 1,141 (2023) · low 29 (2007)2025

MAUDE reports naming product code CGA, 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
20077122229
2008656237
200910155475
201081226172
201192173423
2012101230233
201334413172
201452652122
201541506 (2)155
20164157236
20172—092
20182—069
20192—1116
20202—068
20211—048
20221—0272
2023424931,141
20242—0266
20250—059
20261—0—

What is it indicated for?

The GAL-lA Blood Glucose Monitoring System is intended for the quantitative measurement of glucose in fresh capillary whole blood samples drawn from the fingertips, forearm, or palm. Alternative site testing should be performed only during steady-state (when glucose is not changing rapidly). Testing is done outside the body (In Vitro diagnostic use). It is indicated for lay use by people with diabetes, as an aid to monitoring levels in Diabetes Mellitus…

Read the full statement (161 words)

The GAL-lA Blood Glucose Monitoring System is intended for the quantitative measurement of glucose in fresh capillary whole blood samples drawn from the fingertips, forearm, or palm. Alternative site testing should be performed only during steady-state (when glucose is not changing rapidly). Testing is done outside the body (In Vitro diagnostic use). It is indicated for lay use by people with diabetes, as an aid to monitoring levels in Diabetes Mellitus and should only be used by a single patient and it should not be shared. It is not indicated for the diagnosis or screening of diabetes or for neonatal use.

The GAL-IA Blood Glucose Test Strips are to be used with the GAL-IA Blood Glucose Meter to quantitatively measure glucose in capillary whole blood taken from fingertips, palm, or forearm. Alternative site testing should be performed only during steady-state (when glucose is not changing rapidly). They are not indicated for the diagnosis or screening of diabetes or for neonatal use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K113208: Gal-1A Blood Glucose Monitoring System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113208

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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