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FDA 510(k)

MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT

K-Number: K864829 · 1987-01-12

ApplicantProfessional Instruments Co.
Decision Date1987-01-12
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT is the device name listed in this FDA 510(k) record. The listed applicant is Professional Instruments Co.. It received FDA 510(k) clearance on 1987-01-12 under 510(k) number K864829. 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 MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT?

MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT is a medical device that received FDA 510(k) clearance on 1987-01-12. The listed applicant is Professional Instruments Co.. The 510(k) number is K864829.

When did MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT receive FDA 510(k) clearance?

MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT received FDA 510(k) clearance on 1987-01-12, under 510(k) number K864829.

Who is the listed applicant for MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT?

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

What is the FDA product code for MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT?

The FDA product code for MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT is BXN.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Professional Instruments Co. 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.

K864830TEFLON-COATED HYPODERMIC NEEDLES/REGIONAL BLOCKK810206DUAL TYPE ELECTRODE

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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