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FDA 510(k)

SUN BED BY VERRE ET QUARTZ UVA-FRANCE

K-Number: K833229 · 1984-01-27

ApplicantH & M Douglas Enterprises, Inc.
Decision Date1984-01-27
Product CodeFTZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUN BED BY VERRE ET QUARTZ UVA-FRANCE is the device name listed in this FDA 510(k) record. The listed applicant is H & M Douglas Enterprises, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K833229. The device is classified under product code FTZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUN BED BY VERRE ET QUARTZ UVA-FRANCE?

SUN BED BY VERRE ET QUARTZ UVA-FRANCE is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is H & M Douglas Enterprises, Inc.. The 510(k) number is K833229.

When did SUN BED BY VERRE ET QUARTZ UVA-FRANCE receive FDA 510(k) clearance?

SUN BED BY VERRE ET QUARTZ UVA-FRANCE received FDA 510(k) clearance on 1984-01-27, under 510(k) number K833229.

Who is the listed applicant for SUN BED BY VERRE ET QUARTZ UVA-FRANCE?

The FDA 510(k) record lists H & M Douglas Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUN BED BY VERRE ET QUARTZ UVA-FRANCE?

The FDA product code for SUN BED BY VERRE ET QUARTZ UVA-FRANCE is FTZ.

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Related Devices (Code: FTZ)

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.

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