SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVA
K-Number: K852321 · 1985-07-11
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Device Summary
Frequently Asked Questions
What is the SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVA?
SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVA is a medical device that received FDA 510(k) clearance on 1985-07-11. The listed applicant is Sylvania Lighting Products. The 510(k) number is K852321.
When did SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVA receive FDA 510(k) clearance?
SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVA received FDA 510(k) clearance on 1985-07-11, under 510(k) number K852321.
Who is the listed applicant for SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVA?
The FDA 510(k) record lists Sylvania Lighting Products as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Sylvania Lighting Products 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.
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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