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FDA 510(k)

MARTANIQUE 7-TUBE RUVA HOME SOLARIUM

K-Number: K845028 · 1985-01-14

ApplicantBainbridge Trading Co., Ltd.
Decision Date1985-01-14
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MARTANIQUE 7-TUBE RUVA HOME SOLARIUM is the device name listed in this FDA 510(k) record. The listed applicant is Bainbridge Trading Co., Ltd.. It received FDA 510(k) clearance on 1985-01-14 under 510(k) number K845028. 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 MARTANIQUE 7-TUBE RUVA HOME SOLARIUM?

MARTANIQUE 7-TUBE RUVA HOME SOLARIUM is a medical device that received FDA 510(k) clearance on 1985-01-14. The listed applicant is Bainbridge Trading Co., Ltd.. The 510(k) number is K845028.

When did MARTANIQUE 7-TUBE RUVA HOME SOLARIUM receive FDA 510(k) clearance?

MARTANIQUE 7-TUBE RUVA HOME SOLARIUM received FDA 510(k) clearance on 1985-01-14, under 510(k) number K845028.

Who is the listed applicant for MARTANIQUE 7-TUBE RUVA HOME SOLARIUM?

The FDA 510(k) record lists Bainbridge Trading Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARTANIQUE 7-TUBE RUVA HOME SOLARIUM?

The FDA product code for MARTANIQUE 7-TUBE RUVA HOME SOLARIUM 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 Bainbridge Trading Co., Ltd. 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.

K845001MARTANIQUE 6-TUBE HOME SOLARIUM

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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