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FDA 510(k)

PERIPHERAL NERVE STIMULATOR MODEL A400

K-Number: K852962 · 1985-12-09

ApplicantFisher & Paykel Allied Products , Ltd.
Decision Date1985-12-09
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERIPHERAL NERVE STIMULATOR MODEL A400 is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Allied Products , Ltd.. It received FDA 510(k) clearance on 1985-12-09 under 510(k) number K852962. 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 A400?

PERIPHERAL NERVE STIMULATOR MODEL A400 is a medical device that received FDA 510(k) clearance on 1985-12-09. The listed applicant is Fisher & Paykel Allied Products , Ltd.. The 510(k) number is K852962.

When did PERIPHERAL NERVE STIMULATOR MODEL A400 receive FDA 510(k) clearance?

PERIPHERAL NERVE STIMULATOR MODEL A400 received FDA 510(k) clearance on 1985-12-09, under 510(k) number K852962.

Who is the listed applicant for PERIPHERAL NERVE STIMULATOR MODEL A400?

The FDA 510(k) record lists Fisher & Paykel Allied Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERIPHERAL NERVE STIMULATOR MODEL A400?

The FDA product code for PERIPHERAL NERVE STIMULATOR MODEL A400 is BXN.

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Other records listing Fisher & Paykel Allied Products , Ltd. as applicant

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K880702MODEL MR430 SPECIAL PURPOSE HUMID. HEATER BASESK872138MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIERK872139MR420 TRANSPORT HUMIDIFIERK863377MR338 SERVO HEATED DELIVERY HUMIDIFIERK870055MR590 DUAL HOSE HEATER POWER PACKK862923MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER

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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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