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FDA 510(k)

ELECTRONEURAL STIMULATOR 12

K-Number: K831487 · 1983-10-28

ApplicantMeridia 12 Corp.
Decision Date1983-10-28
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRONEURAL STIMULATOR 12 is the device name listed in this FDA 510(k) record. The listed applicant is Meridia 12 Corp.. It received FDA 510(k) clearance on 1983-10-28 under 510(k) number K831487. 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 ELECTRONEURAL STIMULATOR 12?

ELECTRONEURAL STIMULATOR 12 is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Meridia 12 Corp.. The 510(k) number is K831487.

When did ELECTRONEURAL STIMULATOR 12 receive FDA 510(k) clearance?

ELECTRONEURAL STIMULATOR 12 received FDA 510(k) clearance on 1983-10-28, under 510(k) number K831487.

Who is the listed applicant for ELECTRONEURAL STIMULATOR 12?

The FDA 510(k) record lists Meridia 12 Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONEURAL STIMULATOR 12?

The FDA product code for ELECTRONEURAL STIMULATOR 12 is GZJ.

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Related Devices (Code: GZJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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