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FDA 510(k)

FLUORESCENT T12 UVA LAMP

K-Number: K900649 · 1990-03-28

ApplicantLight Sources, Inc.
Decision Date1990-03-28
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLUORESCENT T12 UVA LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Light Sources, Inc.. It received FDA 510(k) clearance on 1990-03-28 under 510(k) number K900649. 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 FLUORESCENT T12 UVA LAMP?

FLUORESCENT T12 UVA LAMP is a medical device that received FDA 510(k) clearance on 1990-03-28. The listed applicant is Light Sources, Inc.. The 510(k) number is K900649.

When did FLUORESCENT T12 UVA LAMP receive FDA 510(k) clearance?

FLUORESCENT T12 UVA LAMP received FDA 510(k) clearance on 1990-03-28, under 510(k) number K900649.

Who is the listed applicant for FLUORESCENT T12 UVA LAMP?

The FDA 510(k) record lists Light Sources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUORESCENT T12 UVA LAMP?

The FDA product code for FLUORESCENT T12 UVA LAMP is FTC.

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Other records listing Light Sources, Inc. 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.

K901324U.V. SUNLAMP 95UF-IIK900693U.V. SUNLAMP (U.V. LIGHT, DERMATOLOGIC)K883952U. V. SUNLAMP 95UF-11K874889U.V. SUNLAMP 95 UF-11K870167U.V. SUNLAMP 95UF-11K854004FLUORESCENT T12 UVA TANNING 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

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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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