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FDA 510(k)

NERVE STIMULATOR Q10

K-Number: K843175 · 1984-08-20

ApplicantAcm Systems
Decision Date1984-08-20
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NERVE STIMULATOR Q10 is the device name listed in this FDA 510(k) record. The listed applicant is Acm Systems. It received FDA 510(k) clearance on 1984-08-20 under 510(k) number K843175. 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 NERVE STIMULATOR Q10?

NERVE STIMULATOR Q10 is a medical device that received FDA 510(k) clearance on 1984-08-20. The listed applicant is Acm Systems. The 510(k) number is K843175.

When did NERVE STIMULATOR Q10 receive FDA 510(k) clearance?

NERVE STIMULATOR Q10 received FDA 510(k) clearance on 1984-08-20, under 510(k) number K843175.

Who is the listed applicant for NERVE STIMULATOR Q10?

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

What is the FDA product code for NERVE STIMULATOR Q10?

The FDA product code for NERVE STIMULATOR Q10 is BXN.

Related Clinical Trials

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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

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

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