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FDA 510(k)

NEUROMOD COMFORT WAVE #7721 DUAL-

K-Number: K832238 · 1983-08-31

ApplicantMedtronic Vascular
Decision Date1983-08-31
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMOD COMFORT WAVE #7721 DUAL- is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1983-08-31 under 510(k) number K832238. 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 COMFORT WAVE #7721 DUAL-?

NEUROMOD COMFORT WAVE #7721 DUAL- is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Medtronic Vascular. The 510(k) number is K832238.

When did NEUROMOD COMFORT WAVE #7721 DUAL- receive FDA 510(k) clearance?

NEUROMOD COMFORT WAVE #7721 DUAL- received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832238.

Who is the listed applicant for NEUROMOD COMFORT WAVE #7721 DUAL-?

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 COMFORT WAVE #7721 DUAL-?

The FDA product code for NEUROMOD COMFORT WAVE #7721 DUAL- is GZJ.

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Related Devices (Code: GZJ)

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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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