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FDA 510(k)

SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313

K-Number: K760519 · 1976-09-03

Decision Date1976-09-03
Product CodeIOB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313 is the device name listed in this FDA 510(k) record. The listed applicant is Dermatron Corp.. It received FDA 510(k) clearance on 1976-09-03 under 510(k) number K760519. The device is classified under product code IOB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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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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