510(k) Report

510(k) · Cleared

Cleared

Modification to Galileo Gold

K080181510(k) TraditionalCleared Jun 24, 2008152-day reviewClass II21 CFR 868.5895

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

Hamilton Medical AG · CBK Ventilator, Continuous, Facility Use

Cleared on Jun 24, 2008 as substantially equivalent to K061090 (Hamilton Medical AG, 2006) and 2 other predicates after a 152-day review. Its family tree reaches back 8 generations to 1991. 15 of the 68 devices in its family, counting itself, have a Class I recall. 21 later devices descend from it.

Decided
Jun 24, 2008
Review
152 days
Class
Class II
Product code
CBK
Recalls
None
Predicates
3

Its longest line of descent runs back 8 generations to K902859 (1991). 46 ancestors in all, the oldest K902506 (1991). 21 later devices descend from it, 2 citing it directly. 15 of the 68 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2006: 2 other ancestors2004: 4 other ancestors, 1 with a Class I recall12005: 1 other ancestor2001: 4 other ancestors1998: 5 other ancestors2003: 2 other ancestors, 1 with a Class I recall12002: 2 other ancestors2000: 2 other ancestors, 1 with a Class I recall11999: 3 other ancestors1997: 3 other ancestors1994: 4 other ancestors1996: 2 other ancestors1995: 2 other ancestors1991: 1 other ancestor1992: 1 other ancestor2011: 2 descendants cleared, 1 with a Class I recall12012: 5 descendants cleared, 2 with a Class I recall22013: 2 descendants cleared, 2 with a Class I recall22015: 1 descendant cleared2019: 2 descendants cleared, 1 with a Class I recall12017: 2 descendants cleared, 1 with a Class I recall12016: 1 descendant cleared, 1 with a Class I recall12021: 1 descendant cleared, 1 with a Class I recall12020: 2 descendants cleared, 1 with a Class I recall12024: 2 descendants cleared2026: 1 descendant clearedK902859 · Servo Ventilator 300 · Siemens Life Support Systems · 1991 · recalledK961687 · EVITA 4 · Drager, Inc. · 1996K970460 · Nellcor Puritan Bennett, 840 Ventilator System (Model 840) · Puritan Bennett Corp. · 1998 · Class I recallK984535 · Puritan-Bennett 840 Ventilatory System with Bilevel Option · Puritan Bennett Corp. · 1998 · Class I recallK022679 · Raphael · Hamilton Medical AG · 2003 · recalledK040574 · Galileo Gold · Hamilton Medical, Inc. · 2004K051263 · Evitaxl with Option Smartcare · Drager Medical AG & Co. Kgaa · 2005 · recalledK061090 · Galileo Gold Asv · Hamilton Medical AG · 20061990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors, 1 with a Class I recall12 generations back: 6 other ancestors3 generations back: 12 other ancestors, 1 with a Class I recall14 generations back: 10 other ancestors, 1 with a Class I recall15 generations back: 8 other ancestors 1 generation forward: 2 descendants, 1 with a Class I recall12 generations forward: 4 descendants, 3 with a Class I recall33 generations forward: 6 descendants, 1 with a Class I recall14 generations forward: 6 descendants, 5 with a Class I recall55 generations forward: 3 descendants K061090 · Galileo Gold Asv · Hamilton Medical AG · 2006K051263 · Evitaxl with Option Smartcare · Drager Medical AG & Co. Kgaa · 2005 · recalledK040574 · Galileo Gold · Hamilton Medical, Inc. · 2004K022679 · Raphael · Hamilton Medical AG · 2003 · recalledK984535 · Puritan-Bennett 840 Ventilatory System with Bilevel Option · Puritan Bennett Corp. · 1998 · Class I recallK970460 · Nellcor Puritan Bennett, 840 Ventilator System (Model 840) · Puritan Bennett Corp. · 1998 · Class I recallK961687 · EVITA 4 · Drager, Inc. · 1996K902859 · Servo Ventilator 300 · Siemens Life Support Systems · 1991 · recalled−50+5
  1. Root · 8 generations backK902859 Servo Ventilator 300Siemens Life Support Systems · 1991 · Recalled
  2. 7 generations backK961687 EVITA 4Drager, Inc. · 1996
  3. 6 generations backK970460 Nellcor Puritan Bennett, 840 Ventilator System (Model 840)Puritan Bennett Corp. · 1998 · Recalled (Class I)
  4. 5 generations backK984535 Puritan-Bennett 840 Ventilatory System with Bilevel OptionPuritan Bennett Corp. · 1998 · Recalled (Class I)
  5. 4 generations backK022679 RaphaelHamilton Medical AG · 2003 · Recalled
  6. 3 generations backK040574 Galileo GoldHamilton Medical, Inc. · 2004
  7. 2 generations backK051263 Evitaxl with Option SmartcareDrager Medical AG & Co. Kgaa · 2005 · Recalled
  8. 1 generation backK061090 Galileo Gold AsvHamilton Medical AG · 2006
  9. This deviceK080181 Modification to Galileo GoldHamilton Medical AG · 2008
  10. Descendant · cites it directly · 14 of its ownK103803 Hamilton-G5Hamilton Medical AG · 2011 · Recalled (Class I)
  11. Descendant · cites it directly · 14 of its ownK102775 Hamilton-C2Hamilton Medical AG · 2011
  12. Descendant · 2 generations on · 13 of its ownK112006 Hamilton-TC1Hamilton Medical AG · 2012
  13. Descendant · 3 generations on · 11 of its ownK120670 Hamilton-T1Hamilton Medical AG · 2012 · Recalled (Class I)
  14. Descendant · 2 generations on · 10 of its ownK131774 Hamilton-G5Hamilton Medical AG · 2013 · Recalled (Class I)

Showing 5 of 21 descendants. See all descendants

Descendants cleared per year

2011: 22012: 52013: 22015: 12016: 12017: 22019: 22020: 22021: 12024: 22026: 1
2011high 5 (2012) · low 0 (2014)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 21 · See all
  • K103803Hamilton-G5Hamilton Medical AG · 2011 · cites it directly14descendants
  • K102775Hamilton-C2Hamilton Medical AG · 2011 · cites it directly14descendants
  • K112006Hamilton-TC1Hamilton Medical AG · 2012 · 2 generations on13descendants
  • K120670Hamilton-T1Hamilton Medical AG · 2012 · 3 generations on11descendants
  • K131774Hamilton-G5Hamilton Medical AG · 2013 · 2 generations on10descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K902859Servo Ventilator 300Siemens Life Support Systems19913
−7K961687EVITA 4Drager, Inc.1996—
−6K970460Nellcor Puritan Bennett, 840 Ventilator System (Model 840)Puritan Bennett Corp.1998Class I
−5K984535Puritan-Bennett 840 Ventilatory System with Bilevel OptionPuritan Bennett Corp.1998Class I
−4K022679RaphaelHamilton Medical AG20033
−3K040574Galileo GoldHamilton Medical, Inc.2004—
−2K051263Evitaxl with Option SmartcareDrager Medical AG & Co. Kgaa20051
−1K061090Galileo Gold AsvHamilton Medical AG2006—
0 (this device)K080181Modification to Galileo GoldHamilton Medical AG2008—
+1K103803Hamilton-G5Hamilton Medical AG2011Class I
+1K102775Hamilton-C2Hamilton Medical AG2011—
+2K112006Hamilton-TC1Hamilton Medical AG2012—
+3K120670Hamilton-T1Hamilton Medical AG2012Class I
+2K131774Hamilton-G5Hamilton Medical AG2013Class I

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199210
199440
199520
199620
199730
199850
199930
200021
200140
200220
200321
200441
200510
200620

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201121
201252
201322
201510
201611
201721
201921
202021
202111
202420
202610
FIG. 1 — Lineage of K080181, 1991–2026Source: 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.

15 devices in this family have 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 CBK device

  1. #1 K252663 Inbentus Versatilescore 16.0 · 17 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? (3)

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
*K061090Galileo Gold Asv
Summary page 1
…ontinuous, Facility Use (21 CFR 868.5895, Product Code CBK) HAMILTON GALILEO Gold ASV LEGALLY MARKETED 510(k) Number: K061090 DEVICES TO WHICH MAQUET Servo-i EQUIVALENCE IS 510(k) Number: K041 223 BEING CLAIMED: GE Dat…
Hamilton Medical AG2006—
*K041223Modification to Servo-I Ventilator System, Model 64 87 800 E407E
Summary page 1
…HAMILTON GALILEO Gold ASV LEGALLY MARKETED 510(k) Number: K061090 DEVICES TO WHICH MAQUET Servo-i EQUIVALENCE IS 510(k) Number: K041 223 BEING CLAIMED: GE Datex-Ohmeda Engstr~m Carestation 510(k) Number: K062710…
Maquet Critical Care AB2004Class I
*K062710GE Datex-Ohmeda Engstrom Carestation
Summary page 1
…T Servo-i EQUIVALENCE IS 510(k) Number: K041 223 BEING CLAIMED: GE Datex-Ohmeda Engstr~m Carestation 510(k) Number: K062710 Page I of 2 HAMILTON…
Datex-Ohmeda, Inc.20062

Also cleared against K061090: 3 other devices →

What descends from it? (21)

See all 21

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

NumberDeviceApplicantDecidedDescendants
K103803Hamilton-G5 Class IHamilton Medical AG201114
K102775Hamilton-C2Hamilton Medical AG201114

Has anything in its family been recalled? (15 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.

  • K041223Modification to Servo-I Ventilator System, Model 64 87 800 E407EMaquet Critical Care AB · 2004 · Direct predicate · ◆ in the 2004 ancestors bar of FIG. 11 Class I recall
  • K001646Puritan-Bennett 840 Ventilator System with Neomode OptionPuritan Bennett Corp. · 2000 · 3 generations back · ◆ in the 2000 ancestors bar of FIG. 11 Class I recall
  • K984535Puritan-Bennett 840 Ventilatory System with Bilevel OptionPuritan Bennett Corp. · 1998 · 3 generations back · ◆ on the line of descent in FIG. 11 Class I recall
  • K023366Datex-Ohmeda 7900 Ventilator EnhancementsDatex-Ohmeda, Inc. · 2003 · 4 generations back · ◆ in the 2003 ancestors bar of FIG. 11 Class I recall
  • K970460Nellcor Puritan Bennett, 840 Ventilator System (Model 840)Puritan Bennett Corp. · 1998 · 4 generations back · ◆ on the line of descent in FIG. 11 Class I recall
  • K103803Hamilton-G5Hamilton Medical AG · 2011 · Cites it directly · ◆ in the 2011 descendants bar of FIG. 11 Class I recall
  • K121225Hamilton-C2Hamilton Medical AG · 2012 · 2 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
  • K130178Inspiration Ventilator System 5I/7IeVent Medical, Ltd. · 2013 · 2 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
  • K131774Hamilton-G5Hamilton Medical AG · 2013 · 2 generations on · ◆ in the 2013 descendants bar of FIG. 12 Class I recalls
  • K120670Hamilton-T1Hamilton Medical AG · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
  • K162832731 Series VentilatorsZOLL Medical Corporation · 2017 · 4 generations on · ◆ in the 2017 descendants bar of FIG. 11 Class I recall
  • K181216Hamilton-T1, Hamilton-C1Hamilton Medical AG · 2019 · 4 generations on · ◆ in the 2019 descendants bar of FIG. 15 Class I recalls

Nearest 12 of 15 shown.

What does this lineage say?

  • The line of descent spans 17 years and passes through 6 companies; a new generation was cleared every 1.4 years on median.
  • 20 of the 46 ancestors have a recall of any class; 5 have a Class I recall.
  • Of its descendants, K103803 (Hamilton Medical AG, 2011) has gone furthest, with 14 descendants of its own.
  • 3 other devices also cite its predicate K061090.

How does its category compare?

All CBK devices

CBK Ventilator, Continuous, Facility Use: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · CBK

4in 2025

2007: 112008: 182009: 122010: 142011: 132012: 172013: 52014: 52015: 72016: 42017: 62018: 42019: 82020: 52021: 62023: 52024: 92025: 42026 (partial year): 3
2007high 18 (2008) · low 0 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CBK

163in 2025

2007: 142 days median2008: 115 days median2009: 122 days median2010: 150 days median2011: 192 days median2012: 207 days median2013: 277 days median2014: 439 days median2015: 266 days median2016: 323 days median2017: 280 days median2018: 183 days median2019: 435 days median2020: 176 days median2021: 267 days median2023: 309 days median2024: 203 days median2025: 163 days median2026 (partial year): 235 days median
2007high 439 (2014) · low 115 (2008)2026

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

Recalls per year · CBK

14in 2024

2007: 172008: 232009: 82010: 92011: 122012: 2, 1 Class I2013: 5, 2 Class I2014: 5, 4 Class I2015: 6, 4 Class I2016: 4, 1 Class I2017: 12018: 3, 3 Class I2019: 14, 13 Class I2020: 42021: 21, 19 Class I2022: 8, 4 Class I2023: 4, 3 Class I2024: 14, 14 Class I2026 (partial year): 15, 13 Class I
2007high 23 (2008) · low 0 (2025)2026

Class I (81 since 2007) Class II/III not classified

Adverse event reports per year · CBK

13,991in 2025

2007: 1,5312008: 1,9332009: 1,7662010: 1,7992011: 1,8772012: 5,5092013: 7,9212014: 7,6002015: 11,8762016: 16,0562017: 14,4512018: 9,8492019: 9,1002020: 11,0962021: 13,3222022: 15,9742023: 24,9282024: 20,3362025: 13,991
2007high 24,928 (2023) · low 1,531 (2007)2025

MAUDE reports naming product code CBK, 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
200711142171,531
200818115231,933
20091212281,766
20101415091,799
201113192121,877
2012172072 (1)5,509
201352775 (2)7,921
201454395 (4)7,600
201572666 (4)11,876
201643234 (1)16,056
20176280114,451
201841833 (3)9,849
2019843514 (13)9,100
20205176411,096
2021626721 (19)13,322
20220—8 (4)15,974
202353094 (3)24,928
2024920314 (14)20,336
20254163013,991
2026323515 (13)—

What is it indicated for?

The GALILEO Gold ventilator is intended to provide positive pressure ventilatory support to adult, pediatric, infant, and neonatal patients.

The device is intended for use in the hospital and institutional environment where healthcare professionals provide patient care, including use at the patient bedside and for intrafacility transport, provided compressed gas is supplied.

The device is not intended for transportation outside the hospital or for use in the home environment.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K080181: Modification to Galileo Gold.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K080181

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