SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313
K-Number: K760519 · 1976-09-03
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Device Summary
Frequently Asked Questions
What is the SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313?
SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313 is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Dermatron Corp.. The 510(k) number is K760519.
When did SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313 receive FDA 510(k) clearance?
SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313 received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760519.
Who is the listed applicant for SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313?
The FDA 510(k) record lists Dermatron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313?
The FDA product code for SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313 is IOB.
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 Dermatron Corp. 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.
Related Devices (Code: IOB)
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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