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FDA 510(k)

PHILIPS UV-A SOLARIUM TYPE HP 3150

K-Number: K851534 · 1985-05-01

ApplicantPhilips Int'L B.V.
Decision Date1985-05-01
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHILIPS UV-A SOLARIUM TYPE HP 3150 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 1985-05-01 under 510(k) number K851534. 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 3150?

PHILIPS UV-A SOLARIUM TYPE HP 3150 is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Philips Int'L B.V.. The 510(k) number is K851534.

When did PHILIPS UV-A SOLARIUM TYPE HP 3150 receive FDA 510(k) clearance?

PHILIPS UV-A SOLARIUM TYPE HP 3150 received FDA 510(k) clearance on 1985-05-01, under 510(k) number K851534.

Who is the listed applicant for PHILIPS UV-A SOLARIUM TYPE HP 3150?

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 3150?

The FDA product code for PHILIPS UV-A SOLARIUM TYPE HP 3150 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

View all 11 devices →

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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