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FDA 510(k)

ULTRAVIOLET RAD-EMITTING LAMP

K-Number: K771077 · 1977-06-24

ApplicantLee Pharmaceuticals
Decision Date1977-06-24
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ULTRAVIOLET RAD-EMITTING LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K771077. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAVIOLET RAD-EMITTING LAMP?

ULTRAVIOLET RAD-EMITTING LAMP is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K771077.

When did ULTRAVIOLET RAD-EMITTING LAMP receive FDA 510(k) clearance?

ULTRAVIOLET RAD-EMITTING LAMP received FDA 510(k) clearance on 1977-06-24, under 510(k) number K771077.

Who is the listed applicant for ULTRAVIOLET RAD-EMITTING LAMP?

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

What is the FDA product code for ULTRAVIOLET RAD-EMITTING LAMP?

The FDA product code for ULTRAVIOLET RAD-EMITTING LAMP is EBZ.

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Other records listing Lee Pharmaceuticals 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.

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Related Devices (Code: EBZ)

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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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