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FDA 510(k)

NEUROMOD COMPLEMENT #7724 DUAL CHANNEL

K-Number: K823742 · 1983-01-21

ApplicantMedtronic Vascular
Decision Date1983-01-21
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMOD COMPLEMENT #7724 DUAL CHANNEL is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1983-01-21 under 510(k) number K823742. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMOD COMPLEMENT #7724 DUAL CHANNEL?

NEUROMOD COMPLEMENT #7724 DUAL CHANNEL is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Medtronic Vascular. The 510(k) number is K823742.

When did NEUROMOD COMPLEMENT #7724 DUAL CHANNEL receive FDA 510(k) clearance?

NEUROMOD COMPLEMENT #7724 DUAL CHANNEL received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823742.

Who is the listed applicant for NEUROMOD COMPLEMENT #7724 DUAL CHANNEL?

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

What is the FDA product code for NEUROMOD COMPLEMENT #7724 DUAL CHANNEL?

The FDA product code for NEUROMOD COMPLEMENT #7724 DUAL CHANNEL is GZJ.

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Related Devices (Code: GZJ)

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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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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