510(k) · Cleared
ClearedSleepImage System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Mycardio, LLC Dba Sleepimage. · MNR Ventilatory Effort Recorder
Cleared on Aug 14, 2019 as substantially equivalent to K163696 (Mycardio, LLC Dba Sleepimage., 2017) after a 324-day review. Its family tree reaches back 8 generations to 1992. 2 later devices descend from it.
- Decided
- Aug 14, 2019
- Review
- 324 days
- Class
- Class II
- Product code
- MNR
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 8 generations to K913396 (1992). 29 ancestors in all. 2 later devices descend from it, 2 citing it directly.
- Root · 8 generations backK913396 Cannula Style ThermocouplesPro-Tech, Inc. · 1992
- 7 generations backK982293 Pressure Transducer Airflow SensorPro-Tech Services, Inc. · 1998
- 6 generations backK020607 Sleepflo, Model 101501Biomec, Inc. · 2002
- 5 generations backK030379 Aplab, Model 801D0030Sector Medical Corp. · 2003
- 4 generations backK041904 Compass F10 SystemMedcare Flaga · 2004
- 3 generations backK073682 Embletta GoldEmbla Systems, Inc. · 2008 · Recalled
- 2 generations backK092003 CPC Sleep Data Recorder, Model M1, and Application SoftwareMyCardio, LLC · 2009
- 1 generation backK163696 SleepImage SystemMycardio, LLC Dba Sleepimage. · 2017
- This deviceK182618 SleepImage SystemMycardio, LLC Dba Sleepimage. · 2019
- Descendant · cites it directly · 0 of its ownK252628 CassieWesper, Inc. · 2026
- Descendant · cites it directly · 0 of its ownK231355 AuroraEnsodata · 2024
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K913396 | Cannula Style Thermocouples | Pro-Tech, Inc. | 1992 | — |
| −7 | K982293 | Pressure Transducer Airflow Sensor | Pro-Tech Services, Inc. | 1998 | — |
| −6 | K020607 | Sleepflo, Model 101501 | Biomec, Inc. | 2002 | — |
| −5 | K030379 | Aplab, Model 801D0030 | Sector Medical Corp. | 2003 | — |
| −4 | K041904 | Compass F10 System | Medcare Flaga | 2004 | — |
| −3 | K073682 | Embletta Gold | Embla Systems, Inc. | 2008 | 1 |
| −2 | K092003 | CPC Sleep Data Recorder, Model M1, and Application Software | MyCardio, LLC | 2009 | — |
| −1 | K163696 | SleepImage System | Mycardio, LLC Dba Sleepimage. | 2017 | — |
| 0 (this device) | K182618 | SleepImage System | Mycardio, LLC Dba Sleepimage. | 2019 | — |
| +1 | K252628 | Cassie | Wesper, Inc. | 2026 | — |
| +1 | K231355 | Aurora | Ensodata | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1992 | 2 | 0 |
| 1995 | 1 | 0 |
| 1996 | 1 | 0 |
| 1998 | 2 | 0 |
| 1999 | 2 | 0 |
| 2000 | 6 | 0 |
| 2001 | 2 | 0 |
| 2002 | 1 | 0 |
| 2003 | 3 | 0 |
| 2004 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2024 | 1 | 0 |
| 2026 | 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 MNR? 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 MNR device
- #1 K244027 Sansa Hsatscore 18.1 · 12 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 |
|---|---|---|---|
| * | K163696 | SleepImage SystemSummary page 4…vice Classification: Class II Classification Panel: Anesthesiology III. PREDICATE DEVICE Device Trade Name: SleepImage System (K163696) IV. DEVICE DESCRIPTION The SleepImage System is a Class II Software as a Medical Device (SaMD), intended to aid… | 2017 |
What descends from it? (2)
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 27 years and passes through 8 companies; a new generation was cleared every 3.9 years on median.
- 2 of the 29 ancestors have a recall of any class.
- Of its descendants, K252628 (Wesper, Inc., 2026) has gone furthest, with 0 descendants of its own.
How does its category compare?
All MNR devicesMNR Ventilatory Effort Recorder: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · MNR
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MNR
165in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MNR
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MNR
43in 2025
MAUDE reports naming product code MNR, 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 | 6 | 124 | 2 | 1 |
| 2008 | 14 | 118 | 0 | 0 |
| 2009 | 8 | 89 | 1 | 0 |
| 2010 | 0 | — | 0 | 1 |
| 2011 | 9 | 90 | 1 | 1 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 4 | 161 | 0 | 0 |
| 2014 | 2 | — | 0 | 1 |
| 2015 | 4 | 229 | 0 | 4 |
| 2016 | 3 | 281 | 0 | 10 |
| 2017 | 4 | 275 | 0 | 4 |
| 2018 | 3 | 147 | 0 | 2 |
| 2019 | 8 | 383 | 0 | 3 |
| 2020 | 5 | 192 | 0 | 5 |
| 2021 | 3 | 137 | 1 | 5 |
| 2022 | 7 | 266 | 0 | 4 |
| 2023 | 6 | 183 | 0 | 13 |
| 2024 | 6 | 217 | 0 | 11 |
| 2025 | 10 | 165 | 0 | 43 |
| 2026 | 5 | 227 | 1 | — |
What is it indicated for?
The SleepImage System is Software as a Medical Device (SaMD) that establishes sleep quality. The SleepImage System analyzes, displays and summarizes Electrocardiogram (ECG) or Plethysmogram (PLETH) data, typically collected during sleep, that is intended for use by or on the order of a Healthcare Professional to aid in the evaluation of sleep disorders, where it may inform or drive clinical management for children, adolescents and adults. The SleepImage…
Read the full statement (113 words)
The SleepImage System is Software as a Medical Device (SaMD) that establishes sleep quality. The SleepImage System analyzes, displays and summarizes Electrocardiogram (ECG) or Plethysmogram (PLETH) data, typically collected during sleep, that is intended for use by or on the order of a Healthcare Professional to aid in the evaluation of sleep disorders, where it may inform or drive clinical management for children, adolescents and adults.
The SleepImage Apnea Hypopnea Index (sAHI), presented when oximeter data is available, is intended to aid healthcare professionals in diagnosis and management of sleep disordered breathing.
The SleepImage System output is not intended to be interpreted or clinical action taken without consultation of a qualified healthcare professional.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K182618 · printed Nov 6, 2026
Cite this page
510(k) Report. “K182618: SleepImage System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K182618
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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