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FDA 510(k)

STIMUPLEX, NERVE STIMULATOR

K-Number: K860126 · 1986-02-28

ApplicantBurron Medical Products, Inc.
Decision Date1986-02-28
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STIMUPLEX, NERVE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1986-02-28 under 510(k) number K860126. 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 STIMUPLEX, NERVE STIMULATOR?

STIMUPLEX, NERVE STIMULATOR is a medical device that received FDA 510(k) clearance on 1986-02-28. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K860126.

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

STIMUPLEX, NERVE STIMULATOR received FDA 510(k) clearance on 1986-02-28, under 510(k) number K860126.

Who is the listed applicant for STIMUPLEX, NERVE STIMULATOR?

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

What is the FDA product code for STIMUPLEX, NERVE STIMULATOR?

The FDA product code for STIMUPLEX, NERVE STIMULATOR is BXN.

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Other records listing Burron Medical Products, Inc. as applicant

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K870403CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTUREK862412INTESTOPLANTK861479CAVAFIX, CENTRAL VENOUS CATHETER KITK851293IMPLANTOFIXK841428JEJUNOSTOMY SET FOR TUBE FEEDINGK834383DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT

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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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