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FDA 510(k)

SUNTAINNING BOOTH

K-Number: K854707 · 1986-01-30

ApplicantDavid Connell
Decision Date1986-01-30
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

SUNTAINNING BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is David Connell. It received FDA 510(k) clearance on 1986-01-30 under 510(k) number K854707. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SUNTAINNING BOOTH?

SUNTAINNING BOOTH is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is David Connell. The 510(k) number is K854707.

When did SUNTAINNING BOOTH receive FDA 510(k) clearance?

SUNTAINNING BOOTH received FDA 510(k) clearance on 1986-01-30, under 510(k) number K854707.

Who is the listed applicant for SUNTAINNING BOOTH?

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

What is the FDA product code for SUNTAINNING BOOTH?

The FDA product code for SUNTAINNING BOOTH is FTC.

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Related Devices (Code: FTC)

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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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