Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MultiStim ECO

K-Number: K162086 · 2017-01-06

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2017-01-06
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MultiStim ECO is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2017-01-06 under 510(k) number K162086. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MultiStim ECO?

MultiStim ECO is a medical device that received FDA 510(k) clearance on 2017-01-06. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K162086.

When did MultiStim ECO receive FDA 510(k) clearance?

MultiStim ECO received FDA 510(k) clearance on 2017-01-06, under 510(k) number K162086.

Who is the listed applicant for MultiStim ECO?

The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MultiStim ECO?

The FDA product code for MultiStim ECO is BXN.

Other records listing PAJUNK GmbH Medizintechnologie as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243690SonoMSKK243682SonoPlex STIM; SonoPlex IIK250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PunctureK243525SonoTAP and SonoTAP IIK241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyK241954SonoBlock; SonoBlock II

View all 21 devices →

Related Devices (Code: BXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K213049STIMPOD NMS450 Nerve StimulatorXavant Technology (Pty), Ltd.K153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑