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FDA 510(k)

ELECTRONIC PAIN RELIEVERS

K-Number: K883811 · 1989-10-24

ApplicantJetco of America
Decision Date1989-10-24
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC PAIN RELIEVERS is the device name listed in this FDA 510(k) record. The listed applicant is Jetco of America. It received FDA 510(k) clearance on 1989-10-24 under 510(k) number K883811. 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 ELECTRONIC PAIN RELIEVERS?

ELECTRONIC PAIN RELIEVERS is a medical device that received FDA 510(k) clearance on 1989-10-24. The listed applicant is Jetco of America. The 510(k) number is K883811.

When did ELECTRONIC PAIN RELIEVERS receive FDA 510(k) clearance?

ELECTRONIC PAIN RELIEVERS received FDA 510(k) clearance on 1989-10-24, under 510(k) number K883811.

Who is the listed applicant for ELECTRONIC PAIN RELIEVERS?

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

What is the FDA product code for ELECTRONIC PAIN RELIEVERS?

The FDA product code for ELECTRONIC PAIN RELIEVERS is 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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