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FDA 510(k)

RELIEF

K-Number: K812567 · 1981-11-10

Decision Date1981-11-10
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

RELIEF is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaceutical Co., Inc.. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K812567. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIEF?

RELIEF is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is American Pharmaceutical Co., Inc.. The 510(k) number is K812567.

When did RELIEF receive FDA 510(k) clearance?

RELIEF received FDA 510(k) clearance on 1981-11-10, under 510(k) number K812567.

Who is the listed applicant for RELIEF?

The FDA 510(k) record lists American Pharmaceutical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIEF?

The FDA product code for RELIEF is LKX.

Related Clinical Trials

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.

Other records listing American Pharmaceutical Co., Inc. as applicant

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.

Related Devices (Code: LKX)

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.

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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