510(k) · Cleared
ClearedPropeller Sensor for Symbicort
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Reciprocal Labs Corporation · CAF Nebulizer (Direct Patient Interface)
Cleared on Mar 26, 2020 as substantially equivalent to K180770 (Reciprocal Labs Corporation, 2018) after a 181-day review. Its family tree reaches back 9 generations to 1982.
- Decided
- Mar 26, 2020
- Review
- 181 days
- Class
- Class II
- Product code
- CAF
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 9 generations to K823423 (1982). 13 ancestors in all. No later device cites it as a predicate yet.
- Root · 9 generations backK823423 Nebulizer Chronolog & InterpreterAdvanced Technology Products, Inc. · 1982
- 5 generations between
- 3 generations backK152882 Propeller SystemReciprocal Labs · 2016
- 2 generations backK161454 Propeller Sensor Model 2015-EReciprocal Labs Corporation · 2016
- 1 generation backK180770 Propeller Sensor for NeohalerReciprocal Labs Corporation · 2018
- This deviceK192724 Propeller Sensor for SymbicortReciprocal Labs Corporation · 2020
Show all 9 generations
- Root · 9 generations backK823423 Nebulizer Chronolog & InterpreterAdvanced Technology Products, Inc. · 1982
- 8 generations backK970344 Mdilog, Model MDC-511Medtrak Technologies, Inc. · 1997
- 7 generations backK091803 Smarttrack SystemNexus6, Ltd. · 2009
- 6 generations backK121609 Asthmapolis SystemReciprocal Labs Corporation · 2012
- 5 generations backK140638 Propeller System - Model 2Reciprocal Labs Corporation · 2014
- 4 generations backK142516 Propeller SystemReciprocal Labs Corporation · 2015
- 3 generations backK152882 Propeller SystemReciprocal Labs · 2016
- 2 generations backK161454 Propeller Sensor Model 2015-EReciprocal Labs Corporation · 2016
- 1 generation backK180770 Propeller Sensor for NeohalerReciprocal Labs Corporation · 2018
- This deviceK192724 Propeller Sensor for SymbicortReciprocal Labs Corporation · 2020
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K823423 | Nebulizer Chronolog & Interpreter | Advanced Technology Products, Inc. | 1982 | — |
| −8 | K970344 | Mdilog, Model MDC-511 | Medtrak Technologies, Inc. | 1997 | — |
| −7 | K091803 | Smarttrack System | Nexus6, Ltd. | 2009 | — |
| −6 | K121609 | Asthmapolis System | Reciprocal Labs Corporation | 2012 | — |
| −5 | K140638 | Propeller System - Model 2 | Reciprocal Labs Corporation | 2014 | — |
| −4 | K142516 | Propeller System | Reciprocal Labs Corporation | 2015 | — |
| −3 | K152882 | Propeller System | Reciprocal Labs | 2016 | — |
| −2 | K161454 | Propeller Sensor Model 2015-E | Reciprocal Labs Corporation | 2016 | — |
| −1 | K180770 | Propeller Sensor for Neohaler | Reciprocal Labs Corporation | 2018 | — |
| 0 (this device) | K192724 | Propeller Sensor for Symbicort | Reciprocal Labs Corporation | 2020 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 2 | 0 |
| 1999 | 1 | 0 |
| 2015 | 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 CAF? 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 CAF device
- #1 K260270 FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)score 13.2 · 7 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 |
|---|---|---|---|
| * | K180770 | Propeller Sensor for NeohalerSummary page 6…5.1 Page 1 of 7 510(k) K192724 Premarket Notification Reciprocal Labs Corporation, Propeller Sensor Model 2018-S Substantially K180770 Propeller Sensor Model 2017-B Equivalent Devices: Indications For The Propeller System includes the Propeller Sensor Model Use… | 2018 |
What descends from it?
No later submission names this one as a predicate yet.
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 38 years and passes through 5 companies; a new generation was cleared every 1.7 years on median.
- None of the 13 ancestors has a recall.
How does its category compare?
All CAF devicesCAF Nebulizer (Direct Patient Interface): FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · CAF
7in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · CAF
211in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · CAF
1in 2018
Class I (13 since 2007) Class II/III not classified
Adverse event reports per year · CAF
191in 2025
MAUDE reports naming product code CAF, 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 | 18 | 98 | 1 | 26 |
| 2008 | 12 | 123 | 0 | 11 |
| 2009 | 8 | 163 | 0 | 15 |
| 2010 | 10 | 114 | 0 | 37 |
| 2011 | 10 | 157 | 1 | 237 |
| 2012 | 9 | 126 | 0 | 138 |
| 2013 | 9 | 238 | 0 | 217 |
| 2014 | 9 | 151 | 5 | 123 |
| 2015 | 8 | 186 | 3 | 166 |
| 2016 | 5 | 186 | 1 | 201 |
| 2017 | 8 | 253 | 14 (13) | 256 |
| 2018 | 9 | 161 | 1 | 162 |
| 2019 | 3 | 266 | 0 | 185 |
| 2020 | 6 | 219 | 0 | 117 |
| 2021 | 8 | 324 | 0 | 161 |
| 2022 | 4 | 176 | 0 | 55 |
| 2023 | 8 | 279 | 0 | 107 |
| 2024 | 4 | 251 | 0 | 102 |
| 2025 | 7 | 211 | 0 | 191 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
The Propeller System includes the Propeller Sensor Model 2018-S. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed pMDI usage for the Symbicort device. The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the…
Read the full statement (299 words)
The Propeller System includes the Propeller Sensor Model 2018-S. The sensor is an accessory device intended for single-patient use to assist physicians and patients in recording and monitoring the actuations of prescribed pMDI usage for the Symbicort device.
The Propeller Mobile Application records, stores, and transmits usage events from Propeller Sensors, or via manual user entry, to a remote storage system. With the Propeller Mobile Application the user can review information collected from the pMDI sensor, and report and review symptoms and other information about their disease management and its impact. The user may also share their information with their caregivers, physician, and healthcare providers.
The Propeller Web Application is software that, like the Propeller Mobile Application, is intended to allow users to review the collected information and characteristics of their pMDI and its use, to capture other patient-reported information and outcomes, and to allow that information to be shared with their caregivers, physicians, and health care providers.
When used with a prescribed pMDI, the system can report on information captured during the normal course of use, such as the time between actuations that can be helpful in assessing pMDI technique.
The Propeller System is intended to be used in populations from Child (›2 years) to Adult.
The Propeller System can be used both indoors and outdoors; home, work, and clinical settings, as well as on aircraft.
The Propeller System may also be used in clinical trials where researchers need to know information about the use of pMDI medication(s) by a participant.
The output of the Propeller System is not intended to diagnose or replace a diagnosis provided by a licensed physician. The Propeller System is not intended for use as an pMDI dose counter, nor is it intended to indicate the quantity of medication remaining in an pMDI.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K192724 · printed Nov 6, 2026
Cite this page
510(k) Report. “K192724: Propeller Sensor for Symbicort.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192724
Report an extraction error
Are you the manufacturer?
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