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FDA 510(k)

RAMI ULTRAVIOLET A BOOTH

K-Number: K801751 · 1980-09-16

ApplicantRami-Tan
Decision Date1980-09-16
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RAMI ULTRAVIOLET A BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Rami-Tan. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801751. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAMI ULTRAVIOLET A BOOTH?

RAMI ULTRAVIOLET A BOOTH is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Rami-Tan. The 510(k) number is K801751.

When did RAMI ULTRAVIOLET A BOOTH receive FDA 510(k) clearance?

RAMI ULTRAVIOLET A BOOTH received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801751.

Who is the listed applicant for RAMI ULTRAVIOLET A BOOTH?

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

What is the FDA product code for RAMI ULTRAVIOLET A BOOTH?

The FDA product code for RAMI ULTRAVIOLET A BOOTH is LEJ.

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.

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Other records listing Rami-Tan 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.

K801752RAMI TAN ULTRAVIOLET B BOOTH

Related Devices (Code: LEJ)

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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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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