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FDA 510(k)

THE INGLEFIELD MAGIC RING

K-Number: K823056 · 1982-11-03

ApplicantThe Inglefield Co.
Decision Date1982-11-03
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE INGLEFIELD MAGIC RING is the device name listed in this FDA 510(k) record. The listed applicant is The Inglefield Co.. It received FDA 510(k) clearance on 1982-11-03 under 510(k) number K823056. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE INGLEFIELD MAGIC RING?

THE INGLEFIELD MAGIC RING is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is The Inglefield Co.. The 510(k) number is K823056.

When did THE INGLEFIELD MAGIC RING receive FDA 510(k) clearance?

THE INGLEFIELD MAGIC RING received FDA 510(k) clearance on 1982-11-03, under 510(k) number K823056.

Who is the listed applicant for THE INGLEFIELD MAGIC RING?

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

What is the FDA product code for THE INGLEFIELD MAGIC RING?

The FDA product code for THE INGLEFIELD MAGIC RING is FMF.

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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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