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FDA 510(k)

UVB LIGHT BOX - UVB LIGHT BOOTH

K-Number: K792500 · 1980-02-19

ApplicantSun Shanty, Inc.
Decision Date1980-02-19
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UVB LIGHT BOX - UVB LIGHT BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Sun Shanty, Inc.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K792500. 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 UVB LIGHT BOX - UVB LIGHT BOOTH?

UVB LIGHT BOX - UVB LIGHT BOOTH is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Sun Shanty, Inc.. The 510(k) number is K792500.

When did UVB LIGHT BOX - UVB LIGHT BOOTH receive FDA 510(k) clearance?

UVB LIGHT BOX - UVB LIGHT BOOTH received FDA 510(k) clearance on 1980-02-19, under 510(k) number K792500.

Who is the listed applicant for UVB LIGHT BOX - UVB LIGHT BOOTH?

The FDA 510(k) record lists Sun Shanty, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UVB LIGHT BOX - UVB LIGHT BOOTH?

The FDA product code for UVB LIGHT BOX - UVB LIGHT BOOTH is FTC.

Related Clinical Trials

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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Other records listing Sun Shanty, Inc. 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.

K832482COMBO UVB/UVA TANNING BOOTHS 8-40-12-36K837032UVB LIGHT BOX TANNING BOOTHK813307UVA HEX UNIT

Related Devices (Code: FTC)

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.

K254234Phototherapy System (DUV-COMBO)Choyang Medics Co., Ltd.K253871Klär Lite (RCW-KL1000)Radcliffe Watts, LLCK250425Ultraviolet Phototherapy DeviceAPK Technology Co., Ltd.K244022308nm UV Phototherapy System (UV-K); 308nm UV Phototherapy System (UV-X); 308nm UV Phototherapy System (UV-Y); 308nm UV Phototherapy System (UV-Z)Boston Aesthetics, Inc.K242977308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-5000K)Xuzhou Kernel Medical Equipment Co., Ltd.K242908UV Phototherapy Device (Group A: SQ308PCHFD, SQ308PCQFD, SQ308PCPFD, SQ308PCNFD, SQ308PCMFD); UV Phototherapy Device (Group B: SQ308PHTFF, SQ308PHSFF, SQ308PHRFF, SQ308PHZFG, SQ308PPUFF, SQ308PPVFF, SQ308PPWFG)Shanghai Sigma High-Tech Co., Ltd.

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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