510(k) · Cleared
ClearedMedibyte, Model MP8
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Braebon Medical Corp. · MNR Ventilatory Effort Recorder
Cleared on Sep 6, 2006 as substantially equivalent to K031202 (Braebon Medical Corp., 2003) and 3 other predicates after a 76-day review. Its family tree reaches back 3 generations to 1998.
- Decided
- Sep 6, 2006
- Review
- 76 days
- Class
- Class II
- Product code
- MNR
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 3 generations to K981445 (1998). 9 ancestors in all, the oldest K982216 (1998). No later device cites it as a predicate yet.
- Root · 3 generations backK981445 Ultima Airflow Sensor, 0510Braebon Medical Corp. · 1998
- 2 generations backK984431 Ultima Airflow Pressure SensorBraebon Medical Corp. · 1998
- 1 generation backK031202 Medipalm-20Braebon Medical Corp. · 2003
- This deviceK061764 Medibyte, Model MP8Braebon Medical Corp. · 2006
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K981445 | Ultima Airflow Sensor, 0510 | Braebon Medical Corp. | 1998 | — |
| −2 | K984431 | Ultima Airflow Pressure Sensor | Braebon Medical Corp. | 1998 | — |
| −1 | K031202 | Medipalm-20 | Braebon Medical Corp. | 2003 | — |
| 0 (this device) | K061764 | Medibyte, Model MP8 | Braebon Medical Corp. | 2006 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 1 | 0 |
| 2002 | 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? (4)
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 |
|---|---|---|---|
| * | K031202 | Medipalm-20Summary page 2…dicate Device Equivalence We are claiming substantial equivalence to the following devices all manufactured and sold by BRAEBON Medical Corporation: 1. MediPalm®; K031202, Braebon Medical Corporation 2. Ultima Airflow Pressure Sensor; K984431, BRAEBON Medical Corporation 3. Ultima Respir… | 2003 |
| * | K984431 | Ultima Airflow Pressure SensorSummary page 2…wing devices all manufactured and sold by BRAEBON Medical Corporation: 1. MediPalm®; K031202, Braebon Medical Corporation 2. Ultima Airflow Pressure Sensor; K984431, BRAEBON Medical Corporation 3. Ultima Respiratory Effort Sensor; K982216, Braebon Medical Corporation 4. Ultima Snor… | 1998 |
| * | K982216 | Ultima Respiratory Effort Sensor Models 0520 and 0522Summary page 2…MediPalm®; K031202, Braebon Medical Corporation 2. Ultima Airflow Pressure Sensor; K984431, BRAEBON Medical Corporation 3. Ultima Respiratory Effort Sensor; K982216, Braebon Medical Corporation 4. Ultima Snore Microphone; K020312, Braebon Medical Corporation 8.0 Similarities and Differe… | 1998 |
| * | K020312 | Ultima Snoring Mike, Model 0540Summary page 2…w Pressure Sensor; K984431, BRAEBON Medical Corporation 3. Ultima Respiratory Effort Sensor; K982216, Braebon Medical Corporation 4. Ultima Snore Microphone; K020312, Braebon Medical Corporation 8.0 Similarities and Differences Between Subject and Predicate Devices Intended Use… | 2002 |
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 8 years and passes through 1 company; a new generation was cleared every 3.4 years on median.
- None of the 9 ancestors has a recall.
- 2 other devices also cite its predicate K031202.
How does its category compare?
All MNR devicesMNR Ventilatory Effort Recorder: FDA decisions, review times, recalls and adverse event reports over 20 years.
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 MediByte TM is a portable sleep data recorder used to
record physiological signals during sleep while the patient
is either at home or in a clinical environment. The data is
downloaded after the recording is completed and the auto
assist software enables the trained human professional -
typically a Registered Sleep Technologist or Medical
Doctor - to verify the results of the study and generate a
report.
Target Population: Children and adult patients who are screened during sleep
disorder studies.
Environment of Use The majority of the screenings occur either in the home at
in a clinical setting.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K061764 · printed Nov 5, 2026
Cite this page
510(k) Report. “K061764: Medibyte, Model MP8.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K061764
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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