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FDA 510(k)

PERIPHERAL NERVE STIMULATOR, MODEL A-200

K-Number: K822157 · 1982-07-30

ApplicantP.B. Services
Decision Date1982-07-30
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERIPHERAL NERVE STIMULATOR, MODEL A-200 is the device name listed in this FDA 510(k) record. The listed applicant is P.B. Services. It received FDA 510(k) clearance on 1982-07-30 under 510(k) number K822157. 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 PERIPHERAL NERVE STIMULATOR, MODEL A-200?

PERIPHERAL NERVE STIMULATOR, MODEL A-200 is a medical device that received FDA 510(k) clearance on 1982-07-30. The listed applicant is P.B. Services. The 510(k) number is K822157.

When did PERIPHERAL NERVE STIMULATOR, MODEL A-200 receive FDA 510(k) clearance?

PERIPHERAL NERVE STIMULATOR, MODEL A-200 received FDA 510(k) clearance on 1982-07-30, under 510(k) number K822157.

Who is the listed applicant for PERIPHERAL NERVE STIMULATOR, MODEL A-200?

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

What is the FDA product code for PERIPHERAL NERVE STIMULATOR, MODEL A-200?

The FDA product code for PERIPHERAL NERVE STIMULATOR, MODEL A-200 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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