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FDA 510(k)

SUN BEDS

K-Number: K841614 · 1984-05-16

ApplicantSunworld Corp.
Decision Date1984-05-16
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 Sunworld Corp.. It received FDA 510(k) clearance on 1984-05-16 under 510(k) number K841614. 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 1984-05-16. The listed applicant is Sunworld Corp.. The 510(k) number is K841614.

When did SUN BEDS receive FDA 510(k) clearance?

SUN BEDS received FDA 510(k) clearance on 1984-05-16, under 510(k) number K841614.

Who is the listed applicant for SUN BEDS?

The FDA 510(k) record lists Sunworld Corp. 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.

Other records listing Sunworld Corp. 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.

K861636MIAMI-SUNNY

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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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