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FDA 510(k)

NERVE STIMULATORS

K-Number: K771237 · 1977-08-02

ApplicantRule Medical Instruments, Inc.
Decision Date1977-08-02
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NERVE STIMULATORS is the device name listed in this FDA 510(k) record. The listed applicant is Rule Medical Instruments, Inc.. It received FDA 510(k) clearance on 1977-08-02 under 510(k) number K771237. 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 STIMULATORS?

NERVE STIMULATORS is a medical device that received FDA 510(k) clearance on 1977-08-02. The listed applicant is Rule Medical Instruments, Inc.. The 510(k) number is K771237.

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

NERVE STIMULATORS received FDA 510(k) clearance on 1977-08-02, under 510(k) number K771237.

Who is the listed applicant for NERVE STIMULATORS?

The FDA 510(k) record lists Rule Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NERVE STIMULATORS?

The FDA product code for NERVE STIMULATORS 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.

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Other records listing Rule Medical Instruments, Inc. 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.

K791199ANESTHESIA OXYGEN ANALYZER MODEL 101K782074VENTILATOR, MODEL AVA-1, ADULTK771217ANESTHESIA RESPIRATOR

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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