510(k) · Cleared
ClearedZoll Rescuenetlink
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Zoll Medical Corporation, World Wide Headquarters · MSX System, Network And Communication, Physiological Monitors
Cleared on Oct 27, 2011 as substantially equivalent to K102757 (Physio-Control, Inc., 2010) after a 171-day review. Its family tree reaches back 5 generations to 1997. 5 later devices descend from it.
- Decided
- Oct 27, 2011
- Review
- 171 days
- Class
- Class II
- Product code
- MSX
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K971723 (1997). 6 ancestors in all. 5 later devices descend from it, 2 citing it directly.
- Root · 5 generations backK971723 Fastak Suture Anchor (11.7MM)/(7.5MM)Arthrex, Inc. · 1997
- 4 generations backK051219 PushlockArthrex, Inc. · 2005
- 3 generations backK073509 Twinfix PK FP Suture AnchorSmith & Nephew, Inc. · 2008
- 2 generations backK093925 Lifenet SystemPhysio-Control, Inc. · 2010
- 1 generation backK102757 Lifenet SystemPhysio-Control, Inc. · 2010
- This deviceK111296 Zoll RescuenetlinkZoll Medical Corporation, World Wide Headquarters · 2011
- Descendant · cites it directly · 2 of its ownK141774 Zoll X SeriesZOLL Medical Corporation · 2014
- Descendant · 2 generations on · 1 of its ownK202375 ZOLL Propaq MZOLL Medical Corporation · 2021
- Descendant · cites it directly · 1 of its ownK133484 Zoll X SeriesZoll Medical Corp · 2014
- Descendant · 3 generations on · 0 of its ownK233354 WVSM Pro (Series) (500-0030-XX)Athena Gtx, Inc. · 2024
- Descendant · 2 generations on · 0 of its ownK142915 ZOLL X SeriesZOLL Medical Corporation · 2014
Most influential descendants
Showing 5 of 5 · See all- K141774Zoll X SeriesZOLL Medical Corporation · 2014 · cites it directly2descendants
- K202375ZOLL Propaq MZOLL Medical Corporation · 2021 · 2 generations on1descendant
- K133484Zoll X SeriesZoll Medical Corp · 2014 · cites it directly1descendant
- K233354WVSM Pro (Series) (500-0030-XX)Athena Gtx, Inc. · 2024 · 3 generations on0descendants
- K142915ZOLL X SeriesZOLL Medical Corporation · 2014 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K971723 | Fastak Suture Anchor (11.7MM)/(7.5MM) | Arthrex, Inc. | 1997 | — |
| −4 | K051219 | Pushlock | Arthrex, Inc. | 2005 | — |
| −3 | K073509 | Twinfix PK FP Suture Anchor | Smith & Nephew, Inc. | 2008 | — |
| −2 | K093925 | Lifenet System | Physio-Control, Inc. | 2010 | — |
| −1 | K102757 | Lifenet System | Physio-Control, Inc. | 2010 | — |
| 0 (this device) | K111296 | Zoll Rescuenetlink | Zoll Medical Corporation, World Wide Headquarters | 2011 | — |
| +1 | K141774 | Zoll X Series | ZOLL Medical Corporation | 2014 | — |
| +2 | K202375 | ZOLL Propaq M | ZOLL Medical Corporation | 2021 | — |
| +1 | K133484 | Zoll X Series | Zoll Medical Corp | 2014 | — |
| +3 | K233354 | WVSM Pro (Series) (500-0030-XX) | Athena Gtx, Inc. | 2024 | — |
| +2 | K142915 | ZOLL X Series | ZOLL Medical Corporation | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 3 | 0 |
| 2021 | 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.
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 K242750 Central Stationscore 21.5 · 31 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K102757 | Lifenet SystemSummary page 7…and functions of the proposed RescueNet Link are substantially equivalent to the corresponding features and functions of the Physio-Control LIFENET System (K1 02757, cleared for use on 11/5/2010). Comparison of Technological Characteristics RescueNet Link features and functions are simil… | 2010 |
What descends from it? (5)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 14 years and passes through 4 companies; a new generation was cleared every 1.9 years on median.
- None of the 6 ancestors has a recall.
- Of its descendants, K141774 (ZOLL Medical Corporation, 2014) has gone furthest, with 2 descendants of its own.
- 1 other device also cites its predicate K102757.
How does its category compare?
All MSX devicesMSX System, Network And Communication, Physiological Monitors: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · MSX
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MSX
295in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MSX
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MSX
19in 2025
MAUDE reports naming product code MSX, 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 | 4 | 58 | 1 | 5 |
| 2008 | 1 | — | 1 | 6 |
| 2009 | 1 | — | 2 | 7 |
| 2010 | 3 | 43 | 1 | 14 |
| 2011 | 7 | 72 | 1 | 3 |
| 2012 | 4 | 145 | 2 | 4 |
| 2013 | 2 | — | 0 | 17 |
| 2014 | 3 | 165 | 0 | 32 |
| 2015 | 5 | 138 | 2 | 31 |
| 2016 | 3 | 174 | 0 | 11 |
| 2017 | 2 | — | 2 | 16 |
| 2018 | 4 | 111 | 1 | 15 |
| 2019 | 4 | 92 | 0 | 15 |
| 2020 | 5 | 193 | 0 | 25 |
| 2021 | 3 | 227 | 0 | 17 |
| 2022 | 5 | 177 | 1 | 18 |
| 2023 | 3 | 244 | 0 | 10 |
| 2024 | 4 | 212 | 0 | 32 |
| 2025 | 4 | 295 | 1 | 19 |
| 2026 | 5 | 145 | 2 | — |
What is it indicated for?
RescueNet Link is intended for use in the collection and display of data that is entered by a user (caregiver), or captured from specified medical devices or from a vehicle navigation system. RescueNet Link is indicated for use by health care providers whenever there is a need for collection and display of patient, care reporting and transport data.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K111296 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111296: Zoll Rescuenetlink.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111296
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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