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FDA 510(k)

PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP

K-Number: K850205 · 1985-02-21

ApplicantPhilips Int'L B.V.
Decision Date1985-02-21
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Philips Int'L B.V.. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K850205. 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 PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP?

PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Philips Int'L B.V.. The 510(k) number is K850205.

When did PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP receive FDA 510(k) clearance?

PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850205.

Who is the listed applicant for PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP?

The FDA 510(k) record lists Philips Int'L B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP?

The FDA product code for PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP is FTC.

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Other records listing Philips Int'L B.V. 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.

K920134PHILIPS 41 SERIES RAINBOWK920142PHILIPS M60 SERIESK852348PHILIPS SOLARIUM HP 3134K851533PHILIPS UV-A SDARIUM TYPE HP 3148(CFR 21 SUNLAMPK851536PHILIPS UV-A SOLARIUM TYPE HP 3141K851535PHILIPS UV-A SOLARIUM TYPE HP 3140

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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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