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FDA 510(k)

PAJUNK MULTISTIM SENSOR NERVE STIMULATORS

K-Number: K061172 · 2006-10-17

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2006-10-17
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PAJUNK MULTISTIM SENSOR NERVE STIMULATORS 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 2006-10-17 under 510(k) number K061172. 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 PAJUNK MULTISTIM SENSOR NERVE STIMULATORS?

PAJUNK MULTISTIM SENSOR NERVE STIMULATORS is a medical device that received FDA 510(k) clearance on 2006-10-17. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K061172.

When did PAJUNK MULTISTIM SENSOR NERVE STIMULATORS receive FDA 510(k) clearance?

PAJUNK MULTISTIM SENSOR NERVE STIMULATORS received FDA 510(k) clearance on 2006-10-17, under 510(k) number K061172.

Who is the listed applicant for PAJUNK MULTISTIM SENSOR NERVE STIMULATORS?

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 PAJUNK MULTISTIM SENSOR NERVE STIMULATORS?

The FDA product code for PAJUNK MULTISTIM SENSOR NERVE STIMULATORS is BXN.

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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.K162086MultiStim ECOPAJUNK GmbH MedizintechnologieK153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINSunmed, LLCK111985MYOGUIDE SYSTEM MODEL 8008Intronix Technologies Corp.K110118STIMTRODE SINGLE USE NERVE STIMULATORXavant Technology (Pty), 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.

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