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FDA 510(k)

LAMP, FLOURESCENT BLACK, HIGH OUTPUT

K-Number: K760471 · 1976-09-15

ApplicantDermatron Corp.
Decision Date1976-09-15
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAMP, FLOURESCENT BLACK, HIGH OUTPUT is the device name listed in this FDA 510(k) record. The listed applicant is Dermatron Corp.. It received FDA 510(k) clearance on 1976-09-15 under 510(k) number K760471. 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 LAMP, FLOURESCENT BLACK, HIGH OUTPUT?

LAMP, FLOURESCENT BLACK, HIGH OUTPUT is a medical device that received FDA 510(k) clearance on 1976-09-15. The listed applicant is Dermatron Corp.. The 510(k) number is K760471.

When did LAMP, FLOURESCENT BLACK, HIGH OUTPUT receive FDA 510(k) clearance?

LAMP, FLOURESCENT BLACK, HIGH OUTPUT received FDA 510(k) clearance on 1976-09-15, under 510(k) number K760471.

Who is the listed applicant for LAMP, FLOURESCENT BLACK, HIGH OUTPUT?

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

What is the FDA product code for LAMP, FLOURESCENT BLACK, HIGH OUTPUT?

The FDA product code for LAMP, FLOURESCENT BLACK, HIGH OUTPUT 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 Dermatron 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.

K770862BLACK LAMPS,F72T12/BL/HOK761094UVA PHOTOTHERAPY SYSTEMK760482SUNLAMP (F40-UVB & F20-UVB)K760519SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313

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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