510(k) Report

510(k) · Cleared

Cleared

Infinity Gateway Suite

K203579510(k) TraditionalCleared Jun 7, 2022547-day reviewClass II21 CFR 870.2300

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

Draeger Medical Systems, Inc. · MSX System, Network And Communication, Physiological Monitors

Cleared on Jun 7, 2022 as substantially equivalent to K043549 (Draeger Medical Systems, Inc., 2005) after a 547-day review. Its family tree reaches back 5 generations to 1990. 1 later device descends from it.

Decided
Jun 7, 2022
Review
547 days
Class
Class II
Product code
MSX
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K900598 (1990). 9 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 5 generations backK900598 Tramscope SystemMarquette Electronics, Inc. · 1990
  2. 4 generations backK955059 Olympus Comm. NTWK., SC 3000 WKST. & Remote Display, R 100 RecorderSiemens Medical Solutions USA, Inc. · 1996
  3. 3 generations backK014213 Siemens Infinity Gateway SuiteSiemens Medical Solutions USA, Inc. · 2002
  4. 2 generations backK030657 Siemens Infinity Gateway Suite, Model VF2Siemens Medical Solutions · 2003
  5. 1 generation backK043549 Infinity Gateway Suite, VF4Draeger Medical Systems, Inc. · 2005
  6. This deviceK203579 Infinity Gateway SuiteDraeger Medical Systems, Inc. · 2022
  7. Descendant · cites it directly · 0 of its ownK233834 Infinity Gateway SuiteDraeger Medical Systems, Inc. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K233834Infinity Gateway SuiteDraeger Medical Systems, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K900598Tramscope SystemMarquette Electronics, Inc.1990—
−4K955059Olympus Comm. NTWK., SC 3000 WKST. & Remote Display, R 100 RecorderSiemens Medical Solutions USA, Inc.1996—
−3K014213Siemens Infinity Gateway SuiteSiemens Medical Solutions USA, Inc.2002—
−2K030657Siemens Infinity Gateway Suite, Model VF2Siemens Medical Solutions2003—
−1K043549Infinity Gateway Suite, VF4Draeger Medical Systems, Inc.2005—
0 (this device)K203579Infinity Gateway SuiteDraeger Medical Systems, Inc.2022—
+1K233834Infinity Gateway SuiteDraeger Medical Systems, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199020
199110
199310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K203579, 1990–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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 MSX? 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 MSX device

  1. #1 K242750 Central Stationscore 21.5 · 31 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K043549Infinity Gateway Suite, VF4
Summary page 5
…LNX Regulatory Class: II Regulation Number: §870.1025 III. Predicate Device The Infinity® Gateway Suite, VF4 K043549 cleared on January 21, 2005. 510(k) Trade Name Manufacturer Product Code/Common Name Regula…
Draeger Medical Systems, Inc.2005—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K233834Infinity Gateway SuiteDraeger Medical Systems, Inc.20240

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 32 years and passes through 4 companies; a new generation was cleared every 5.6 years on median.
  • None of the 9 ancestors has a recall.
  • Of its descendants, K233834 (Draeger Medical Systems, Inc., 2024) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MSX devices

MSX System, Network And Communication, Physiological Monitors: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · MSX

4in 2025

2007: 42008: 12009: 12010: 32011: 72012: 42013: 22014: 32015: 52016: 32017: 22018: 42019: 42020: 52021: 32022: 52023: 32024: 42025: 42026 (partial year): 5
2007high 7 (2011) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSX

295in 2025

2007: 58 days median2010: 43 days median2011: 72 days median2012: 145 days median2014: 165 days median2015: 138 days median2016: 174 days median2018: 111 days median2019: 92 days median2020: 193 days median2021: 227 days median2022: 177 days median2023: 244 days median2024: 212 days median2025: 295 days median2026 (partial year): 145 days median
2007high 295 (2025) · low 43 (2010)2026

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

Recalls per year · MSX

1in 2025

2007: 12008: 12009: 22010: 12011: 12012: 22015: 22017: 22018: 12022: 12025: 12026 (partial year): 2
2007high 2 (2009) · low 0 (2013)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MSX

19in 2025

2007: 52008: 62009: 72010: 142011: 32012: 42013: 172014: 322015: 312016: 112017: 162018: 152019: 152020: 252021: 172022: 182023: 102024: 322025: 19
2007high 32 (2014) · low 3 (2011)2025

MAUDE reports naming product code MSX, 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
200745815
20081—16
20091—27
2010343114
201177213
2012414524
20132—017
20143165032
20155138231
20163174011
20172—216
20184111115
2019492015
20205193025
20213227017
20225177118
20233244010
20244212032
20254295119
202651452—

What is it indicated for?

The Infinity Gateway software applications are intended to provide clinicians with the capability of viewing patient data remotely via the Infinity Network and for the data exchange of select clinical and administrative information between the Infinity Network and the hospital network.

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. “K203579: Infinity Gateway Suite.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K203579

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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