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FDA 510(k)

SOLAR PACIFIC UVA SUNLAMP DEVICE

K-Number: K801520 · 1980-08-20

ApplicantSolar Pacific
Decision Date1980-08-20
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOLAR PACIFIC UVA SUNLAMP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Solar Pacific. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801520. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLAR PACIFIC UVA SUNLAMP DEVICE?

SOLAR PACIFIC UVA SUNLAMP DEVICE is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Solar Pacific. The 510(k) number is K801520.

When did SOLAR PACIFIC UVA SUNLAMP DEVICE receive FDA 510(k) clearance?

SOLAR PACIFIC UVA SUNLAMP DEVICE received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801520.

Who is the listed applicant for SOLAR PACIFIC UVA SUNLAMP DEVICE?

The FDA 510(k) record lists Solar Pacific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLAR PACIFIC UVA SUNLAMP DEVICE?

The FDA product code for SOLAR PACIFIC UVA SUNLAMP DEVICE is LEJ.

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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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