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FDA 510(k)

ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9

K-Number: K852534 · 1985-11-08

ApplicantR. A. Fischer Co. Corp.
Decision Date1985-11-08
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 is the device name listed in this FDA 510(k) record. The listed applicant is R. A. Fischer Co. Corp.. It received FDA 510(k) clearance on 1985-11-08 under 510(k) number K852534. 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 ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9?

ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K852534.

When did ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 receive FDA 510(k) clearance?

ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 received FDA 510(k) clearance on 1985-11-08, under 510(k) number K852534.

Who is the listed applicant for ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9?

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

What is the FDA product code for ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9?

The FDA product code for ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 is FTC.

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Other records listing R. A. Fischer Co. 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.

K964208MD-1A GALVANIC UNITK954031COMPU-BLEND EPILATORK895365MD-2 IONTOPHORESIS UNITK893389MODEL SE-5 EPILATORK884079MODEL CBX EPILATORK871372CB-7 ELECTRONIC EPILATOR

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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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