PORTASUN MODEL 600/LI SUNLAMP
K-Number: K852149 · 1985-05-31
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Device Summary
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
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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