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FDA 510(k)

MEDICAL SUNLAMP FOR PHOTOTHERAPY

K-Number: K915426 · 1992-03-04

Decision Date1992-03-04
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDICAL SUNLAMP FOR PHOTOTHERAPY is the device name listed in this FDA 510(k) record. The listed applicant is American Sunlight, Inc.. It received FDA 510(k) clearance on 1992-03-04 under 510(k) number K915426. 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 MEDICAL SUNLAMP FOR PHOTOTHERAPY?

MEDICAL SUNLAMP FOR PHOTOTHERAPY is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is American Sunlight, Inc.. The 510(k) number is K915426.

When did MEDICAL SUNLAMP FOR PHOTOTHERAPY receive FDA 510(k) clearance?

MEDICAL SUNLAMP FOR PHOTOTHERAPY received FDA 510(k) clearance on 1992-03-04, under 510(k) number K915426.

Who is the listed applicant for MEDICAL SUNLAMP FOR PHOTOTHERAPY?

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

What is the FDA product code for MEDICAL SUNLAMP FOR PHOTOTHERAPY?

The FDA product code for MEDICAL SUNLAMP FOR PHOTOTHERAPY 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.

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.

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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