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FDA 510(k)

SUN TANNING BED MODEL EC-3RF

K-Number: K853692 · 1985-10-01

ApplicantMottek Intl. Corp.
Decision Date1985-10-01
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUN TANNING BED MODEL EC-3RF is the device name listed in this FDA 510(k) record. The listed applicant is Mottek Intl. Corp.. It received FDA 510(k) clearance on 1985-10-01 under 510(k) number K853692. 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 TANNING BED MODEL EC-3RF?

SUN TANNING BED MODEL EC-3RF is a medical device that received FDA 510(k) clearance on 1985-10-01. The listed applicant is Mottek Intl. Corp.. The 510(k) number is K853692.

When did SUN TANNING BED MODEL EC-3RF receive FDA 510(k) clearance?

SUN TANNING BED MODEL EC-3RF received FDA 510(k) clearance on 1985-10-01, under 510(k) number K853692.

Who is the listed applicant for SUN TANNING BED MODEL EC-3RF?

The FDA 510(k) record lists Mottek Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUN TANNING BED MODEL EC-3RF?

The FDA product code for SUN TANNING BED MODEL EC-3RF is FTC.

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Other records listing Mottek Intl. 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.

K860198MODEL 7500/000 KETTLER HOLIDAY SOLAR SUN TANNINGK855162ULTRAVIOLET SUN TANNING UNIT KETTLER HOLIDAY SOLARK854932ECUMOL ULTRAVIOLET FACE TANNING UNITSK853177ECUMOL ULTRAVIOLET SUNTANNNING BEDSK852243KETTLER ULTRAVIOLET SUNTANNING BENCHES & LIFTSK852053ORIGINAL ULTRAVIOLET SUNTANNING LAMP

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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