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FDA 510(k)

TANARAMA

K-Number: K812543 · 1981-10-08

ApplicantMarketing Consultants of America
Decision Date1981-10-08
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TANARAMA is the device name listed in this FDA 510(k) record. The listed applicant is Marketing Consultants of America. It received FDA 510(k) clearance on 1981-10-08 under 510(k) number K812543. 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 TANARAMA?

TANARAMA is a medical device that received FDA 510(k) clearance on 1981-10-08. The listed applicant is Marketing Consultants of America. The 510(k) number is K812543.

When did TANARAMA receive FDA 510(k) clearance?

TANARAMA received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812543.

Who is the listed applicant for TANARAMA?

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

What is the FDA product code for TANARAMA?

The FDA product code for TANARAMA 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 Marketing Consultants 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.

K812603TANARAMA

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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