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FDA 510(k)

PHOTOTHERAPEUTIX MODEL 2400B

K-Number: K933954 · 1995-02-21

ApplicantAvex Industries , Ltd.
Decision Date1995-02-21
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHOTOTHERAPEUTIX MODEL 2400B is the device name listed in this FDA 510(k) record. The listed applicant is Avex Industries , Ltd.. It received FDA 510(k) clearance on 1995-02-21 under 510(k) number K933954. 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 PHOTOTHERAPEUTIX MODEL 2400B?

PHOTOTHERAPEUTIX MODEL 2400B is a medical device that received FDA 510(k) clearance on 1995-02-21. The listed applicant is Avex Industries , Ltd.. The 510(k) number is K933954.

When did PHOTOTHERAPEUTIX MODEL 2400B receive FDA 510(k) clearance?

PHOTOTHERAPEUTIX MODEL 2400B received FDA 510(k) clearance on 1995-02-21, under 510(k) number K933954.

Who is the listed applicant for PHOTOTHERAPEUTIX MODEL 2400B?

The FDA 510(k) record lists Avex Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOTOTHERAPEUTIX MODEL 2400B?

The FDA product code for PHOTOTHERAPEUTIX MODEL 2400B 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 Avex Industries , Ltd. 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.

K935525PHOTOTHERAPEUTIX MODEL 2480ABK933953PHOTOTHERAPEUTIX MODEL 1650BK933952PHOTOTHERAPEUTIX MODEL 800BK935524PHOTOTHERAPEUTIX MODEL 3200AK935526PHOTOTHERAPEUTIX MODEL 1600B

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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