510(k) Report

510(k) · Cleared

Cleared

Vpap Iii ST-a

K033276510(k) TraditionalCleared Jun 7, 2004241-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

Resmed, Ltd. · MNS Ventilator, Continuous, Non-Life-Supporting

Cleared on Jun 7, 2004 as substantially equivalent to K974417 (Resmed Corp, 1998) after a 241-day review. Its family tree reaches back 1 generation to 1998. 10 of the 70 devices in its family, counting itself, have a Class I recall. 68 later devices descend from it.

Decided
Jun 7, 2004
Review
241 days
Class
Class II
Product code
MNS
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K974417 (1998). 68 later devices descend from it, 5 citing it directly. 10 of the 70 devices in this family, counting this one, have a Class I recall.

Descendants, by year cleared 2005: 1 descendant cleared2010: 5 descendants cleared, 1 with a Class I recall12006: 1 descendant cleared2009: 7 descendants cleared, 2 with a Class I recall22012: 12 descendants cleared, 2 with a Class I recall22011: 7 descendants cleared, 2 with a Class I recall22008: 2 descendants cleared2016: 4 descendants cleared2007: 3 descendants cleared2013: 4 descendants cleared, 1 with a Class I recall12014: 3 descendants cleared2024: 3 descendants cleared2022: 1 descendant cleared2017: 1 descendant cleared2026: 2 descendants cleared2018: 2 descendants cleared2020: 4 descendants cleared2015: 1 descendant cleared2019: 1 descendant cleared, 1 with a Class I recall12025: 2 descendants cleared2021: 1 descendant cleared, 1 with a Class I recall12023: 1 descendant clearedK974417 · Sullivan Vpap II ST-a Nasal Vpap System · Resmed Corp · 19981995200020052010201520202025
Descendants, by generation 1 generation forward: 5 descendants2 generations forward: 16 descendants3 generations forward: 15 descendants, 3 with a Class I recall34 generations forward: 16 descendants, 3 with a Class I recall35 generations forward: 9 descendants, 3 with a Class I recall36 generations forward: 5 descendants, 1 with a Class I recall17 generations forward: 2 descendants K974417 · Sullivan Vpap II ST-a Nasal Vpap System · Resmed Corp · 19980+5
  1. Root · 1 generation backK974417 Sullivan Vpap II ST-a Nasal Vpap SystemResmed Corp · 1998
  2. This deviceK033276 Vpap Iii ST-aResmed, Ltd. · 2004
  3. Descendant · cites it directly · 53 of its ownK060105 Vpap Iii ST-a/Kidsta Mask SystemResmed, Ltd. · 2006
  4. Descendant · cites it directly · 36 of its ownK051364 Vpap AdaptResmed, Ltd. · 2005
  5. Descendant · 2 generations on · 30 of its ownK063533 Bipap SynchronyRespironics, Inc. · 2007
  6. Descendant · 3 generations on · 28 of its ownK071509 Bipap Synchrony 2 Ventilatory Support SystemRespironics Inc., Sleep & Home Respiratory Group · 2007 · Recalled
  7. Descendant · 2 generations on · 20 of its ownK103167 Stellar 150Resmed Germany, Inc. · 2011

Showing 5 of 68 descendants. See all descendants

Descendants cleared per year

2005: 12006: 12007: 32008: 22009: 72010: 52011: 72012: 122013: 42014: 32015: 12016: 42017: 12018: 22019: 12020: 42021: 12022: 12023: 12024: 32025: 22026: 2
2005high 12 (2012) · low 1 (2005)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 68 · See all
  • K060105Vpap Iii ST-a/Kidsta Mask SystemResmed, Ltd. · 2006 · cites it directly53descendants
  • K051364Vpap AdaptResmed, Ltd. · 2005 · cites it directly36descendants
  • K063533Bipap SynchronyRespironics, Inc. · 2007 · 2 generations on30descendants
  • K071509Bipap Synchrony 2 Ventilatory Support SystemRespironics Inc., Sleep & Home Respiratory Group · 2007 · 3 generations on28descendants
  • K103167Stellar 150Resmed Germany, Inc. · 2011 · 2 generations on20descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K974417Sullivan Vpap II ST-a Nasal Vpap SystemResmed Corp1998—
0 (this device)K033276Vpap Iii ST-aResmed, Ltd.2004—
+1K060105Vpap Iii ST-a/Kidsta Mask SystemResmed, Ltd.2006—
+1K051364Vpap AdaptResmed, Ltd.2005—
+2K063533Bipap SynchronyRespironics, Inc.2007—
+3K071509Bipap Synchrony 2 Ventilatory Support SystemRespironics Inc., Sleep & Home Respiratory Group20072
+2K103167Stellar 150Resmed Germany, Inc.2011—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
200610
200730
200820
200972
201051
201172
2012122
201341
201430
201510
201640
201710
201820
201911
202040
202111
202210
202310
202430
202520
202620
FIG. 1 — Lineage of K033276, 1998–2026Source: 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.

10 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 MNS device

  1. #1 K251661 Mariana Minerva; Mariana Nimbusscore 14.2 · 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? (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
*K974417Sullivan Vpap II ST-a Nasal Vpap System
Summary page 4
…Variable Positive Air Pressure (VPAP) System / Classification Name: Continuous Ventilator, Non-life-support Predicate Devices: VPAP IIST-A (K974417) Device Description: The VPAP Ill ST-A provides a mode of non-invasive positive pr…
Resmed Corp1998—

Also cleared against K974417: 1 other device →

What descends from it? (68)

See all 68

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

NumberDeviceApplicantDecidedDescendants
K060105Vpap Iii ST-a/Kidsta Mask SystemResmed, Ltd.200653
K051364Vpap AdaptResmed, Ltd.200536
K092186Vpap TXResmed, Ltd.200918
K113288Vpap ST-aResmed, Ltd.20127
K093731Vpap Iii ST-aResmed, Ltd.20100

Has anything in its family been recalled? (10 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.

  • K090539Bipap Autosv AdvancedRespironics Inc., Sleep & Home Respiratory Group · 2009 · 3 generations on · ◆ in the 2009 descendants bar of FIG. 12 Class I recalls
  • K090248Bipap AutosvRespironics Inc., Sleep & Home Respiratory Group · 2009 · 3 generations on · ◆ in the 2009 descendants bar of FIG. 14 Class I recalls
  • K113053Bipap a 30 Ventilatory Support SystemRespironics, Inc. · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 15 Class I recalls
  • K092818Bipap Avaps Ventilatory Support SystemRespironics, Inc. · 2010 · 4 generations on · ◆ in the 2010 descendants bar of FIG. 11 Class I recall
  • K121623Bipap a 40 Ventilatory Support SystemRespironics, Inc. · 2012 · 4 generations on · ◆ in the 2012 descendants bar of FIG. 13 Class I recalls
  • K122715Stellar 150Resmed Germany, Inc. · 2013 · 4 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
  • K102465Bipap Avaps Ventilatory Support SystemRespironics, Inc. · 2011 · 5 generations on · ◆ in the 2011 descendants bar of FIG. 11 Class I recall
  • K111378Oximetry Interface KitPhilips Respironics, Inc. · 2011 · 5 generations on · ◆ in the 2011 descendants bar of FIG. 11 Class I recall
  • K181166Trilogy EvoRespironics, Inc. · 2019 · 5 generations on · ◆ in the 2019 descendants bar of FIG. 131 Class I recalls
  • K193586Vivo 45 LSBreas Medical AB · 2021 · 6 generations on · ◆ in the 2021 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • Its one ancestor has no recall.
  • Of its descendants, K060105 (Resmed, Ltd., 2006) has gone furthest, with 53 descendants of its own.
  • 1 other device also cites its predicate K974417.

How does its category compare?

All MNS devices

MNS Ventilator, Continuous, Non-Life-Supporting: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MNS

1in 2024

2007: 42009: 42010: 42011: 32012: 52013: 32016: 22017: 12018: 12022: 12023: 12024: 12026 (partial year): 3
2007high 5 (2012) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MNS

115in 2013

2007: 90 days median2009: 92 days median2010: 124 days median2011: 140 days median2012: 111 days median2013: 115 days median2026 (partial year): 269 days median
2007high 269 (2026) · low 90 (2007)2026

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

Recalls per year · MNS

1in 2008

2007: 22008: 12026 (partial year): 1, 1 Class I
2007high 2 (2007) · low 0 (2009)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · MNS

1,790in 2025

2007: 92008: 72009: 82010: 92011: 92012: 122013: 182014: 52015: 502016: 162017: 202018: 222019: 2752020: 642021: 2562022: 2,5142023: 1,3202024: 1,5712025: 1,790
2007high 2,514 (2022) · low 5 (2014)2025

MAUDE reports naming product code MNS, 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
200749029
20080—17
200949208
2010412409
2011314009
20125111012
20133115018
20140—05
20150—050
20162—016
20171—020
20181—022
20190—0275
20200—064
20210—0256
20221—02,514
20231—01,320
20241—01,571
20250—01,790
202632691 (1)—

What is it indicated for?

The VPAP III ST-A system is intended to provide non-invasive ventilation for patients with respiratory insufficiency or obstructive sleep apnea (OSA), in the hospital or home.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K033276: Vpap Iii ST-a.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K033276

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