510(k) Report

510(k) · Cleared

Cleared

MultiStim ECO

K162086510(k) TraditionalCleared Jan 6, 2017163-day reviewClass II21 CFR 868.2775

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

PAJUNK GmbH Medizintechnologie · BXN Stimulator, Nerve, Battery-Powered

Cleared on Jan 6, 2017 as substantially equivalent to K061172 (PAJUNK GmbH Medizintechnologie, 2006) after a 163-day review. Its family tree reaches back 2 generations to 2001.

Decided
Jan 6, 2017
Review
163 days
Class
Class II
Product code
BXN
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K011308 (2001). No later device cites it as a predicate yet.

  1. Root · 2 generations backK011308 MultistimPajunk GmbH · 2001
  2. 1 generation backK061172 Pajunk Multistim Sensor Nerve StimulatorsPAJUNK GmbH Medizintechnologie · 2006
  3. This deviceK162086 MultiStim ECOPAJUNK GmbH Medizintechnologie · 2017
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K011308MultistimPajunk GmbH2001—
−1K061172Pajunk Multistim Sensor Nerve StimulatorsPAJUNK GmbH Medizintechnologie2006—
0 (this device)K162086MultiStim ECOPAJUNK GmbH Medizintechnologie2017—
FIG. 1 — Lineage of K162086, 2001–2017Source: 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 BXN? 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 BXN device

  1. #1 K213049 STIMPOD NMS450 Nerve Stimulatorscore 5.4 · 5 generations · no Class I recall
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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
*K061172Pajunk Multistim Sensor Nerve Stimulators
Summary page 5
…Anesthesiology Predicate Device Information: Device Name: MultiStim SENSOR Document Control Number K061172 PAJUNK MULTISTIM SENSOR NERVE 510(k) title STIMULATORS…
PAJUNK GmbH Medizintechnologie2006—

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 16 years and passes through 2 companies; a new generation was cleared every 10.2 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All BXN devices

BXN Stimulator, Nerve, Battery-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · BXN

1in 2022

2007: 32009: 22010: 12011: 22013: 12014: 12015: 12016: 12017: 12022: 1
2007high 3 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BXN

108in 2007

2007: 108 days median
2007high 108 (2007)2026

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

Recalls per year · BXN

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 · BXN

4in 2024

2007: 12008: 12009: 12010: 22011: 12012: 52013: 12015: 32017: 12021: 22023: 42024: 4
2007high 5 (2012) · low 0 (2014)2025

MAUDE reports naming product code BXN, 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
2007310801
20080—01
20092—01
20101—12
20112—01
20120—05
20131—01
20141—00
20151—03
20161—00
20171—01
20180—00
20190—00
20200—00
20210—02
20221—00
20230—04
20240—04
20250—00
20260—0—

What is it indicated for?

Pajunk's MultiStim ECO is intended for nerve stimulation during anaesthesia delivery; first for identification of peripheral nerves and second for localizations. This device is indicated for adults only.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K162086: MultiStim ECO.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K162086

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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