510(k) Report

510(k) · Cleared

Cleared

Wesper Lab

K221816510(k) TraditionalCleared Mar 9, 2023260-day reviewClass II21 CFR 868.2375

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

Wesper, Inc. · MNR Ventilatory Effort Recorder

Cleared on Mar 9, 2023 as substantially equivalent to K203343 (Wesper, Inc., 2021) after a 260-day review. Its family tree reaches back 8 generations to 1992.

Decided
Mar 9, 2023
Review
260 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. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2004: 1 other ancestor2003: 3 other ancestors1996: 1 other ancestor2002: 1 other ancestor2001: 2 other ancestors2000: 6 other ancestors1999: 2 other ancestors1998: 2 other ancestors1995: 1 other ancestor1992: 2 other ancestorsK913396 · Cannula Style Thermocouples · Pro-Tech, Inc. · 1992K982293 · Pressure Transducer Airflow Sensor · Pro-Tech Services, Inc. · 1998K020607 · Sleepflo, Model 101501 · Biomec, Inc. · 2002K030379 · Aplab, Model 801D0030 · Sector Medical Corp. · 2003K041904 · Compass F10 System · Medcare Flaga · 2004K073682 · Embletta Gold · Embla Systems, Inc. · 2008 · recalledK122516 · Embletta MPR · Embla Systems · 2013 · recalledK203343 · Wesper Lab · Wesper, Inc. · 202119901995200020052010201520202025
  1. Root · 8 generations backK913396 Cannula Style ThermocouplesPro-Tech, Inc. · 1992
  2. 7 generations backK982293 Pressure Transducer Airflow SensorPro-Tech Services, Inc. · 1998
  3. 6 generations backK020607 Sleepflo, Model 101501Biomec, Inc. · 2002
  4. 5 generations backK030379 Aplab, Model 801D0030Sector Medical Corp. · 2003
  5. 4 generations backK041904 Compass F10 SystemMedcare Flaga · 2004
  6. 3 generations backK073682 Embletta GoldEmbla Systems, Inc. · 2008 · Recalled
  7. 2 generations backK122516 Embletta MPREmbla Systems · 2013 · Recalled
  8. 1 generation backK203343 Wesper LabWesper, Inc. · 2021
  9. This deviceK221816 Wesper LabWesper, Inc. · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K913396Cannula Style ThermocouplesPro-Tech, Inc.1992—
−7K982293Pressure Transducer Airflow SensorPro-Tech Services, Inc.1998—
−6K020607Sleepflo, Model 101501Biomec, Inc.2002—
−5K030379Aplab, Model 801D0030Sector Medical Corp.2003—
−4K041904Compass F10 SystemMedcare Flaga2004—
−3K073682Embletta GoldEmbla Systems, Inc.20081
−2K122516Embletta MPREmbla Systems20131
−1K203343Wesper LabWesper, Inc.2021—
0 (this device)K221816Wesper LabWesper, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199220
199510
199610
199820
199920
200060
200120
200210
200330
200410
FIG. 1 — Lineage of K221816, 1992–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K244027 Sansa Hsatscore 18.1 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K203343Wesper Lab
Summary page 4
…quency monitor. Regulation: 21 CFR 868.2375 Regulatory Class: II Product Code: MNR 3. PREDICATE DEVICE  Wesper Lab (K203343) 4. DEVICE DESCRIPTION Wesper Lab (“the device”) is a digital recording device designed to be used under the direction of a phy…
Wesper, Inc.2021—

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 31 years and passes through 8 companies; a new generation was cleared every 4.1 years on median.
  • 3 of the 29 ancestors have a recall of any class.

How does its category compare?

All MNR devices

MNR Ventilatory Effort Recorder: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · MNR

10in 2025

2007: 62008: 142009: 82011: 92012: 12013: 42014: 22015: 42016: 32017: 42018: 32019: 82020: 52021: 32022: 72023: 62024: 62025: 102026 (partial year): 5
2007high 14 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MNR

165in 2025

2007: 124 days median2008: 118 days median2009: 89 days median2011: 90 days median2013: 161 days median2015: 229 days median2016: 281 days median2017: 275 days median2018: 147 days median2019: 383 days median2020: 192 days median2021: 137 days median2022: 266 days median2023: 183 days median2024: 217 days median2025: 165 days median2026 (partial year): 227 days median
2007high 383 (2019) · low 89 (2009)2026

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

Recalls per year · MNR

1in 2021

2007: 22009: 12011: 12021: 12026 (partial year): 1
2007high 2 (2007) · low 0 (2008)2026

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

Adverse event reports per year · MNR

43in 2025

2007: 12010: 12011: 12012: 12014: 12015: 42016: 102017: 42018: 22019: 32020: 52021: 52022: 42023: 132024: 112025: 43
2007high 43 (2025) · low 0 (2008)2025

MAUDE reports naming product code MNR, 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
2007612421
20081411800
200988910
20100—01
201199011
20121—01
2013416100
20142—01
2015422904
20163281010
2017427504
2018314702
2019838303
2020519205
2021313715
2022726604
20236183013
20246217011
202510165043
202652271—

What is it indicated for?

The Wesper Lab is a digital recording device designed to be used under the direction of a physician or trained technician but may be applied by a layperson. Wesper Lab records multiple physiological parameters from a sleeping patient for the purpose of simultaneous or subsequent display of the parameters. The displayed data assists in the identification of sleep apnea by trained personnel. Wesper Lab is intended to be used for adult sleep studies at home or clinical environment. The device does not actively monitor or diagnose the patient and does not issue any alarms.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K221816: Wesper Lab.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K221816

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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