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FDA 510(k)

MULTI-STIMT

K-Number: K840599 · 1984-04-13

ApplicantJoanco Medical Electronics , Ltd.
Decision Date1984-04-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MULTI-STIMT is the device name listed in this FDA 510(k) record. The listed applicant is Joanco Medical Electronics , Ltd.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840599. 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 MULTI-STIMT?

MULTI-STIMT is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Joanco Medical Electronics , Ltd.. The 510(k) number is K840599.

When did MULTI-STIMT receive FDA 510(k) clearance?

MULTI-STIMT received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840599.

Who is the listed applicant for MULTI-STIMT?

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

What is the FDA product code for MULTI-STIMT?

The FDA product code for MULTI-STIMT 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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