Decision Date1984-04-25
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
SUN BEDS is the device name listed in this FDA 510(k) record. The listed applicant is Wakewood Sunbeds. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K840931. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SUN BEDS?
SUN BEDS is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Wakewood Sunbeds. The 510(k) number is K840931.
When did SUN BEDS receive FDA 510(k) clearance?
SUN BEDS received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840931.
Who is the listed applicant for SUN BEDS?
The FDA 510(k) record lists Wakewood Sunbeds as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUN BEDS?
The FDA product code for SUN BEDS is FTC.
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Official Source
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