510(k) Report

510(k) · Cleared

Cleared

Vpap ST

K080131510(k) TraditionalCleared Apr 1, 200874-day reviewClass II21 CFR 868.5905

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

Resmed, Ltd. · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Apr 1, 2008 as substantially equivalent to K062291 (Resmed, Ltd., 2006) and 3 other predicates after a 74-day review. Its family tree reaches back 6 generations to 1997. 38 later devices descend from it.

Decided
Apr 1, 2008
Review
74 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
4

Its longest line of descent runs back 6 generations to K971260 (1997). 12 ancestors in all, the oldest K930656 (1994). 38 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor1996: 1 other ancestor2003: 1 other ancestor2002: 1 other ancestor1998: 1 other ancestor1994: 1 other ancestor2011: 4 descendants cleared2009: 3 descendants cleared2010: 1 descendant cleared2014: 5 descendants cleared2013: 2 descendants cleared2012: 6 descendants cleared2016: 4 descendants cleared2020: 3 descendants cleared2022: 2 descendants cleared2017: 1 descendant cleared2021: 1 descendant cleared2026: 2 descendants cleared2023: 1 descendant cleared2024: 1 descendant cleared2025: 2 descendants clearedK971260 · Sullivan Humidaire Heated Humidifier · Resmed Corp · 1997K013909 · S7 Elite CP AP System · Resmed Corp · 2002K024191 · S7 Elite and Autoset Spirit Cpap Systems with Reslink · Resmed, Ltd. · 2003×2: 2 generations cleared close together, K033841 (2004), K041209 (2004) K071171 · Vpap Auto with H3I · Resmed, Ltd. · 20071990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 2 other ancestors3 generations back: 2 other ancestors 1 generation forward: 5 descendants2 generations forward: 11 descendants3 generations forward: 10 descendants4 generations forward: 7 descendants5 generations forward: 3 descendants6 generations forward: 1 descendant7 generations forward: 1 descendant K071171 · Vpap Auto with H3I · Resmed, Ltd. · 2007K041209 · Resmed S8 Pioneer Cpap System · Resmed, Ltd. · 2004 · recalledK033841 · Resmed S8 Prime Cpap System · Resmed, Ltd. · 2004 · recalledK024191 · S7 Elite and Autoset Spirit Cpap Systems with Reslink · Resmed, Ltd. · 2003K013909 · S7 Elite CP AP System · Resmed Corp · 2002K971260 · Sullivan Humidaire Heated Humidifier · Resmed Corp · 1997−50+5
  1. Root · 6 generations backK971260 Sullivan Humidaire Heated HumidifierResmed Corp · 1997
  2. 5 generations backK013909 S7 Elite CP AP SystemResmed Corp · 2002
  3. 4 generations backK024191 S7 Elite and Autoset Spirit Cpap Systems with ReslinkResmed, Ltd. · 2003
  4. 3 generations backK033841 Resmed S8 Prime Cpap SystemResmed, Ltd. · 2004 · Recalled
  5. 2 generations backK041209 Resmed S8 Pioneer Cpap SystemResmed, Ltd. · 2004 · Recalled
  6. 1 generation backK071171 Vpap Auto with H3IResmed, Ltd. · 2007
  7. This deviceK080131 Vpap STResmed, Ltd. · 2008
  8. Descendant · cites it directly · 31 of its ownK091947 S8 Aspen with H4I PlusResmed, Ltd. · 2009
  9. Descendant · cites it directly · 18 of its ownK092186 Vpap TXResmed, Ltd. · 2009
  10. Descendant · cites it directly · 11 of its ownK102513 S9 Vpap ST with H5IResmed, Ltd. · 2011
  11. Descendant · 2 generations on · 8 of its ownK140124 S9 EloueraResmed Corp · 2014
  12. Descendant · 2 generations on · 7 of its ownK113288 Vpap ST-aResmed, Ltd. · 2012

Showing 5 of 38 descendants. See all descendants

Descendants cleared per year

2009: 32010: 12011: 42012: 62013: 22014: 52016: 42017: 12020: 32021: 12022: 22023: 12024: 12025: 22026: 2
2009high 6 (2012) · low 0 (2015)2026

Most influential descendants

Showing 5 of 38 · See all
  • K091947S8 Aspen with H4I PlusResmed, Ltd. · 2009 · cites it directly31descendants
  • K092186Vpap TXResmed, Ltd. · 2009 · cites it directly18descendants
  • K102513S9 Vpap ST with H5IResmed, Ltd. · 2011 · cites it directly11descendants
  • K140124S9 EloueraResmed Corp · 2014 · 2 generations on8descendants
  • K113288Vpap ST-aResmed, Ltd. · 2012 · 2 generations on7descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K971260Sullivan Humidaire Heated HumidifierResmed Corp1997—
−5K013909S7 Elite CP AP SystemResmed Corp2002—
−4K024191S7 Elite and Autoset Spirit Cpap Systems with ReslinkResmed, Ltd.2003—
−3K033841Resmed S8 Prime Cpap SystemResmed, Ltd.20041
−2K041209Resmed S8 Pioneer Cpap SystemResmed, Ltd.20041
−1K071171Vpap Auto with H3IResmed, Ltd.2007—
0 (this device)K080131Vpap STResmed, Ltd.2008—
+1K091947S8 Aspen with H4I PlusResmed, Ltd.2009—
+1K092186Vpap TXResmed, Ltd.2009—
+1K102513S9 Vpap ST with H5IResmed, Ltd.2011—
+2K140124S9 EloueraResmed Corp2014—
+2K113288Vpap ST-aResmed, Ltd.2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199610
199810
200210
200310
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200930
201010
201140
201260
201320
201450
201640
201710
202030
202110
202220
202310
202410
202520
202620
FIG. 1 — Lineage of K080131, 1997–2026Source: 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.

Planning a device in BZD? 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 BZD device

  1. #1 K250624 myAirscore 15.7 · 12 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? (4)

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
*K062291Vpap Malibu with H2I
Summary page 1
…Common/Usual Name Noncontinuous ventilator (IPPB). Proprietary Name VPAP ST Predicate Device(s) VPAP Malibu (K062291) - Primary S8 Pioneer (K041209) - Secondary Sullivan…
Resmed, Ltd.2006—
*K041209Resmed S8 Pioneer Cpap System
Summary page 1
…). Proprietary Name VPAP ST Predicate Device(s) VPAP Malibu (K062291) - Primary S8 Pioneer (K041209) - Secondary Sullivan VPAP II ST (K961783)- Secondary…
Resmed, Ltd.20041
*K961783Sullivan Vpap II ST Nasal Vpap System
Summary page 1
…VPAP Malibu (K062291) - Primary S8 Pioneer (K041209) - Secondary Sullivan VPAP II ST (K961783)- Secondary VPAP Auto (K071171) - Secondary Reason for submission New Devi…
Resmed, Ltd.1996—
*K071171Vpap Auto with H3I
Summary page 1
…S8 Pioneer (K041209) - Secondary Sullivan VPAP II ST (K961783)- Secondary VPAP Auto (K071171) - Secondary Reason for submission New Device Intended for Use The VPAP ST is indicated for the treatment of O…
Resmed, Ltd.2007—

Also cleared against K062291: 1 other device →

What descends from it? (38)

See all 38

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

NumberDeviceApplicantDecidedDescendants
K091947S8 Aspen with H4I PlusResmed, Ltd.200931
K092186Vpap TXResmed, Ltd.200918
K102513S9 Vpap ST with H5IResmed, Ltd.201111
K091919Devilbiss Intellipap/Sleepcube Bilevel S/STSunrise Medical20091
K093070Devilbiss Intellipap/ Sleepcube Bilevel ST, DV56 ST SeriesSunrise Medical20100

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 2 companies; a new generation was cleared every 12 months on median.
  • 2 of the 12 ancestors have a recall of any class.
  • Of its descendants, K091947 (Resmed, Ltd., 2009) has gone furthest, with 31 descendants of its own.
  • 1 other device also cites its predicate K062291.

How does its category compare?

All BZD devices

BZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · BZD

7in 2025

2007: 212008: 172009: 232010: 122011: 232012: 212013: 232014: 142015: 112016: 122017: 52018: 52019: 62020: 62021: 62022: 42023: 52024: 102025: 72026 (partial year): 10
2007high 23 (2009) · low 4 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZD

189in 2025

2007: 83 days median2008: 108 days median2009: 90 days median2010: 122 days median2011: 125 days median2012: 133 days median2013: 127 days median2014: 172 days median2015: 224 days median2016: 217 days median2017: 221 days median2018: 280 days median2019: 231 days median2020: 137 days median2021: 192 days median2022: 253 days median2023: 204 days median2024: 132 days median2025: 189 days median2026 (partial year): 214 days median
2007high 280 (2018) · low 83 (2007)2026

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

Recalls per year · BZD

8in 2023

2007: 292008: 22009: 12011: 12019: 4, 4 Class I2023: 8, 7 Class I2026 (partial year): 2, 2 Class I
2007high 29 (2007) · low 0 (2010)2026

Class I (13 since 2007) Class II/III not classified

Adverse event reports per year · BZD

60,279in 2025

2007: 652008: 672009: 1472010: 1432011: 1892012: 1392013: 822014: 862015: 1142016: 1182017: 1482018: 1012019: 1882020: 1262021: 6,0662022: 90,7682023: 27,9872024: 68,2622025: 60,279
2007high 90,768 (2022) · low 65 (2007)2025

MAUDE reports naming product code BZD, 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
200721832965
200817108267
200923901147
2010121220143
2011231251189
2012211330139
201323127082
201414172086
2015112240114
2016122170118
201752210148
201852800101
201962314 (4)188
202061370126
2021619206,066
20224253090,768
202352048 (7)27,987
202410132068,262
20257189060,279
2026102142 (2)—

What is it indicated for?

The VPAP ST is indicated for the treatment of Obstructive Sleep Apnea (OSA) in patients weighing more than 66 lb (30 kg). The optional integrated HumidAire 4i is indicated for humidification of the air delivered from a ResMed compatible CPAP therapy device. The VPAP ST and HumidAire 4i are intended for use in the hospital and home.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K080131: Vpap ST.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K080131

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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