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FDA 510(k)

PORTASUN MODEL 600/LI SUNLAMP

K-Number: K852149 · 1985-05-31

Decision Date1985-05-31
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PORTASUN MODEL 600/LI SUNLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Portasun , Ltd.. It received FDA 510(k) clearance on 1985-05-31 under 510(k) number K852149. 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 PORTASUN MODEL 600/LI SUNLAMP?

PORTASUN MODEL 600/LI SUNLAMP is a medical device that received FDA 510(k) clearance on 1985-05-31. The listed applicant is Portasun , Ltd.. The 510(k) number is K852149.

When did PORTASUN MODEL 600/LI SUNLAMP receive FDA 510(k) clearance?

PORTASUN MODEL 600/LI SUNLAMP received FDA 510(k) clearance on 1985-05-31, under 510(k) number K852149.

Who is the listed applicant for PORTASUN MODEL 600/LI SUNLAMP?

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

What is the FDA product code for PORTASUN MODEL 600/LI SUNLAMP?

The FDA product code for PORTASUN MODEL 600/LI SUNLAMP 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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