FDA 510(k)

PAIN-EEZ

K-Number: K922690 · 1992-10-13

ApplicantInternational Center For Nutritional Research

Decision Date1992-10-13

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

PAIN-EEZ is the device name listed in this FDA 510(k) record. The listed applicant is International Center For Nutritional Research. It received FDA 510(k) clearance on 1992-10-13 under 510(k) number K922690. 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 PAIN-EEZ?

PAIN-EEZ is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is International Center For Nutritional Research. The 510(k) number is K922690.

When did PAIN-EEZ receive FDA 510(k) clearance?

PAIN-EEZ received FDA 510(k) clearance on 1992-10-13, under 510(k) number K922690.

Who is the listed applicant for PAIN-EEZ?

The FDA 510(k) record lists International Center For Nutritional Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAIN-EEZ?

The FDA product code for PAIN-EEZ is GZJ.

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

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