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FDA 510(k)

MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM

K-Number: K883868 · 1988-11-28

Decision Date1988-11-28
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Electronics , Ltd.. It received FDA 510(k) clearance on 1988-11-28 under 510(k) number K883868. 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 NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM?

MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM is a medical device that received FDA 510(k) clearance on 1988-11-28. The listed applicant is Fisher & Paykel Electronics , Ltd.. The 510(k) number is K883868.

When did MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM receive FDA 510(k) clearance?

MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM received FDA 510(k) clearance on 1988-11-28, under 510(k) number K883868.

Who is the listed applicant for MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM?

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

What is the FDA product code for MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM?

The FDA product code for MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM 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.

Other records listing Fisher & Paykel Electronics , Ltd. 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.

View all 17 devices →

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.

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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