510(k) Report

510(k) · Cleared

Cleared

Neurovision Medical Motion Sensor

K130570510(k) TraditionalCleared Dec 26, 2013297-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

Neurovision Medical Products, Inc. · BZQ Monitor, Breathing Frequency

Cleared on Dec 26, 2013 as substantially equivalent to K062883 (Gereonics, Inc., 2007) after a 297-day review. Its family tree reaches back 2 generations to 1994.

Decided
Dec 26, 2013
Review
297 days
Class
Class II
Product code
BZQ
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K940014 (1994). No later device cites it as a predicate yet.

  1. Root · 2 generations backK940014 PLM Sensor, Model PLM1Pro-Tech, Inc. · 1994
  2. 1 generation backK062883 Gereonics Ultra-Piezo Limb Movement SensorGereonics, Inc. · 2007
  3. This deviceK130570 Neurovision Medical Motion SensorNeurovision Medical Products, Inc. · 2013
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K940014PLM Sensor, Model PLM1Pro-Tech, Inc.1994—
−1K062883Gereonics Ultra-Piezo Limb Movement SensorGereonics, Inc.2007—
0 (this device)K130570Neurovision Medical Motion SensorNeurovision Medical Products, Inc.2013—
FIG. 1 — Lineage of K130570, 1994–2013Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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 BZQ? 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 BZQ device

  1. #1 K251326 Respiration Rate algorithmscore 20.2 · 30 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K062883Gereonics Ultra-Piezo Limb Movement Sensor
Summary page 1
…The Neurovision Medical Motion Sensor is substantially equivalent to the following predicate devices currently distributed commercially in the U.S.: .K062883; Gereonics Ultra-Piezo Limb Movement Sensor Device Description The Neurovision Medical Motion Sensor is a disposable, mul…
Gereonics, Inc.2007—

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 19 years and passes through 3 companies; a new generation was cleared every 12.6 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All BZQ devices

BZQ Monitor, Breathing Frequency: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · BZQ

7in 2025

2007: 22008: 12009: 32010: 22011: 12012: 22013: 32014: 22016: 22018: 32019: 12020: 22021: 22022: 32023: 12024: 12025: 72026 (partial year): 2
2007high 7 (2025) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZQ

255in 2025

2009: 121 days median2013: 261 days median2018: 198 days median2022: 198 days median2025: 255 days median
2007high 261 (2013) · low 121 (2009)2026

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

Recalls per year · BZQ

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · BZQ

2in 2022

2007: 72009: 12010: 12012: 32017: 112018: 102019: 132020: 102021: 12022: 2
2007high 13 (2019) · low 0 (2008)2025

MAUDE reports naming product code BZQ, 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
20072—07
20081—00
2009312101
20102—11
20111—00
20122—03
2013326100
20142—00
20150—00
20162—00
20170—011
20183198010
20191—013
20202—010
20212—01
2022319802
20231—00
20241—00
2025725500
20262—0—

What is it indicated for?

The Neurovision Medical Motion Sensor is intended to detect, monitor and/or record limb movements on a physiological recorder, in adult patient sleep disorder studies, in a clinical setting.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K130570: Neurovision Medical Motion Sensor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K130570

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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