510(k) · Cleared
ClearedFlight 60 Ventilator, Model F-60
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Flight Medical, Ltd. · CBK Ventilator, Continuous, Facility Use
Cleared on Aug 20, 2010 as substantially equivalent to K992133 (Newport Medical Instruments, Inc., 2000) and 1 other predicate after a 156-day review. Its family tree reaches back 10 generations to 1991. 4 of the 68 devices in its family, counting itself, have a Class I recall. 5 later devices descend from it.
- Decided
- Aug 20, 2010
- Review
- 156 days
- Class
- Class II
- Product code
- CBK
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 10 generations to K902859 (1991). 62 ancestors in all, the oldest K841279 (1984). 5 later devices descend from it, 1 citing it directly. 4 of the 68 devices in this family, counting this one, have a Class I recall.
- Root · 10 generations backK902859 Servo Ventilator 300Siemens Life Support Systems · 1991 · Recalled
- 6 generations between
- 3 generations backK053270 IVENT 201Versamed Medical Systems, Inc. · 2006
- 2 generations backK061627 Modification to I Vent 201Versamed Medical Systems, Inc. · 2006
- 1 generation backK082724 Newport HTS50 Ventilator with Dual Pac Battery SystemNewport Medical Instruments, Inc. · 2008 · Recalled
- This deviceK100753 Flight 60 Ventilator, Model F-60Flight Medical, Ltd. · 2010
- Descendant · cites it directly · 4 of its ownK111683 Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2011
- Descendant · 2 generations on · 3 of its ownK120726 Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2012
- Descendant · 3 generations on · 2 of its ownK130171 Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2014
- Descendant · 4 generations on · 1 of its ownK143035 Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2016
- Descendant · 5 generations on · 0 of its ownK223120 Ventoux VC2; Ventoux VC3Flight Medical Innovations, Ltd. · 2024
Show all 10 generations
- Root · 10 generations backK902859 Servo Ventilator 300Siemens Life Support Systems · 1991 · Recalled
- 9 generations backK960010 Servo Ventilator 300 Computer InterfaceSiemens Elema AB · 1996
- 8 generations backK970839 Servo Ventilator 300ASiemens Elema AB · 1997 · Recalled
- 7 generations backK992788 Bear Cub 750 PSVBear Medical Systems, Inc. · 1999
- 6 generations backK013642 AVEABird Products Corp. · 2002 · Recalled (Class I)
- 5 generations backK032451 Bird Tbird Vela VentilatorBird Products Corp. · 2004 · Recalled
- 4 generations backK052554 Modification to: Ivent 201 Portable VentilatorVersamed Medical Systems, Inc. · 2005
- 3 generations backK053270 IVENT 201Versamed Medical Systems, Inc. · 2006
- 2 generations backK061627 Modification to I Vent 201Versamed Medical Systems, Inc. · 2006
- 1 generation backK082724 Newport HTS50 Ventilator with Dual Pac Battery SystemNewport Medical Instruments, Inc. · 2008 · Recalled
- This deviceK100753 Flight 60 Ventilator, Model F-60Flight Medical, Ltd. · 2010
Class I recalls in this family
Most influential descendants
Showing 5 of 5 · See all- K111683Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2011 · cites it directly4descendants
- K120726Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2012 · 2 generations on3descendants
- K130171Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2014 · 3 generations on2descendants
- K143035Flight 60 VentilatorFlight Medical Innovations, Ltd. · 2016 · 4 generations on1descendant
- K223120Ventoux VC2; Ventoux VC3Flight Medical Innovations, Ltd. · 2024 · 5 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K902859 | Servo Ventilator 300 | Siemens Life Support Systems | 1991 | 3 |
| −9 | K960010 | Servo Ventilator 300 Computer Interface | Siemens Elema AB | 1996 | — |
| −8 | K970839 | Servo Ventilator 300A | Siemens Elema AB | 1997 | 4 |
| −7 | K992788 | Bear Cub 750 PSV | Bear Medical Systems, Inc. | 1999 | — |
| −6 | K013642 | AVEA | Bird Products Corp. | 2002 | Class I |
| −5 | K032451 | Bird Tbird Vela Ventilator | Bird Products Corp. | 2004 | 1 |
| −4 | K052554 | Modification to: Ivent 201 Portable Ventilator | Versamed Medical Systems, Inc. | 2005 | — |
| −3 | K053270 | IVENT 201 | Versamed Medical Systems, Inc. | 2006 | — |
| −2 | K061627 | Modification to I Vent 201 | Versamed Medical Systems, Inc. | 2006 | — |
| −1 | K082724 | Newport HTS50 Ventilator with Dual Pac Battery System | Newport Medical Instruments, Inc. | 2008 | 2 |
| 0 (this device) | K100753 | Flight 60 Ventilator, Model F-60 | Flight Medical, Ltd. | 2010 | — |
| +1 | K111683 | Flight 60 Ventilator | Flight Medical Innovations, Ltd. | 2011 | — |
| +2 | K120726 | Flight 60 Ventilator | Flight Medical Innovations, Ltd. | 2012 | — |
| +3 | K130171 | Flight 60 Ventilator | Flight Medical Innovations, Ltd. | 2014 | — |
| +4 | K143035 | Flight 60 Ventilator | Flight Medical Innovations, Ltd. | 2016 | — |
| +5 | K223120 | Ventoux VC2; Ventoux VC3 | Flight Medical Innovations, Ltd. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1984 | 1 | 0 |
| 1988 | 1 | 0 |
| 1990 | 4 | 0 |
| 1991 | 4 | 0 |
| 1992 | 2 | 0 |
| 1993 | 1 | 0 |
| 1994 | 3 | 0 |
| 1995 | 3 | 0 |
| 1996 | 3 | 0 |
| 1997 | 2 | 0 |
| 1998 | 10 | 2 |
| 1999 | 5 | 0 |
| 2000 | 3 | 0 |
| 2001 | 2 | 0 |
| 2002 | 1 | 0 |
| 2003 | 3 | 1 |
| 2004 | 3 | 0 |
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2012 | 1 | 0 |
| 2014 | 1 | 0 |
| 2016 | 1 | 0 |
| 2024 | 1 | 0 |
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.
4 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 K252663 Inbentus Versatilescore 16.0 · 17 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K992133 | Newport HT50 Ventilator with Humidifier HT50-H, Newport HT50 Ventilator Without…Summary page 1…tilators as class 1I devices (product code 73 CBK and NOU) and they are reviewed by the Anesthesiology panel Predicate Devices: Newport HT50 Ventilator cleared under K992133 and K082724 Device Description: The FLIGHT 60 Ventilator is an electrically powered, microprocessor controlled ventilator wit… | 2000 |
| * | K082724 | Newport HTS50 Ventilator with Dual Pac Battery SystemSummary page 1…class 1I devices (product code 73 CBK and NOU) and they are reviewed by the Anesthesiology panel Predicate Devices: Newport HT50 Ventilator cleared under K992133 and K082724 Device Description: The FLIGHT 60 Ventilator is an electrically powered, microprocessor controlled ventilator with the follow… | 2008 |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K111683 | Flight 60 Ventilator | 2011 | 4 |
Has anything in its family been recalled? (4 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.
- K023366Datex-Ohmeda 7900 Ventilator EnhancementsDatex-Ohmeda, Inc. · 2003 · 4 generations back · ◆ in the 2003 ancestors bar of FIG. 11 Class I recall
- K013642AVEABird Products Corp. · 2002 · 4 generations back · ◆ on the line of descent in FIG. 113 Class I recalls
- K981072Esprit VentilatorRespironics, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
- K970460Nellcor Puritan Bennett, 840 Ventilator System (Model 840)Puritan Bennett Corp. · 1998 · 5 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 19 years and passes through 7 companies; a new generation was cleared every 1.8 years on median.
- 20 of the 62 ancestors have a recall of any class; 4 have a Class I recall.
- Of its descendants, K111683 (Flight Medical Innovations, Ltd., 2011) has gone furthest, with 4 descendants of its own.
- 3 other devices also cite its predicate K992133.
How does its category compare?
All CBK devicesCBK Ventilator, Continuous, Facility Use: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · CBK
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · CBK
163in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · CBK
14in 2024
Class I (81 since 2007) Class II/III not classified
Adverse event reports per year · CBK
13,991in 2025
MAUDE reports naming product code CBK, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 11 | 142 | 17 | 1,531 |
| 2008 | 18 | 115 | 23 | 1,933 |
| 2009 | 12 | 122 | 8 | 1,766 |
| 2010 | 14 | 150 | 9 | 1,799 |
| 2011 | 13 | 192 | 12 | 1,877 |
| 2012 | 17 | 207 | 2 (1) | 5,509 |
| 2013 | 5 | 277 | 5 (2) | 7,921 |
| 2014 | 5 | 439 | 5 (4) | 7,600 |
| 2015 | 7 | 266 | 6 (4) | 11,876 |
| 2016 | 4 | 323 | 4 (1) | 16,056 |
| 2017 | 6 | 280 | 1 | 14,451 |
| 2018 | 4 | 183 | 3 (3) | 9,849 |
| 2019 | 8 | 435 | 14 (13) | 9,100 |
| 2020 | 5 | 176 | 4 | 11,096 |
| 2021 | 6 | 267 | 21 (19) | 13,322 |
| 2022 | 0 | — | 8 (4) | 15,974 |
| 2023 | 5 | 309 | 4 (3) | 24,928 |
| 2024 | 9 | 203 | 14 (14) | 20,336 |
| 2025 | 4 | 163 | 0 | 13,991 |
| 2026 | 3 | 235 | 15 (13) | — |
What is it indicated for?
The FLIGHT 60 Ventilator is intended to provide continuous or intermittent mechanical ventilation support for the care of individuals who require mechanical ventilation. Specifically, the FLIGHT 60 is applicable for adult and pediatric (i.e., infant, child and adolescent) patients, greater than or equal to 10kg (22 Ibs).
The FLIGHT 60 Ventilator is a restricted medical device intended for use by qualified, trained personnel under the direction of a physician; it is suitable for use in hospital, sub-acute, emergency room, and home care environments, as well as for transport and emergency response applications.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K100753 · printed Nov 6, 2026
Cite this page
510(k) Report. “K100753: Flight 60 Ventilator, Model F-60.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K100753
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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