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FDA 510(k)

NORDIC SUN HOME TANNING UNIT

K-Number: K860567 · 1986-03-05

ApplicantNordic Sun Corporation of America
Decision Date1986-03-05
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NORDIC SUN HOME TANNING UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Nordic Sun Corporation of America. It received FDA 510(k) clearance on 1986-03-05 under 510(k) number K860567. 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 NORDIC SUN HOME TANNING UNIT?

NORDIC SUN HOME TANNING UNIT is a medical device that received FDA 510(k) clearance on 1986-03-05. The listed applicant is Nordic Sun Corporation of America. The 510(k) number is K860567.

When did NORDIC SUN HOME TANNING UNIT receive FDA 510(k) clearance?

NORDIC SUN HOME TANNING UNIT received FDA 510(k) clearance on 1986-03-05, under 510(k) number K860567.

Who is the listed applicant for NORDIC SUN HOME TANNING UNIT?

The FDA 510(k) record lists Nordic Sun Corporation of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORDIC SUN HOME TANNING UNIT?

The FDA product code for NORDIC SUN HOME TANNING UNIT 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 Nordic Sun Corporation of America 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.

K860566NORDIC SUN 24 LAMP TANNING BED

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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