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FDA 510(k)

ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72

K-Number: K881923 · 1988-07-07

Decision Date1988-07-07
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72 is the device name listed in this FDA 510(k) record. The listed applicant is Ultraviolet Resources Intl.. It received FDA 510(k) clearance on 1988-07-07 under 510(k) number K881923. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72?

ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72 is a medical device that received FDA 510(k) clearance on 1988-07-07. The listed applicant is Ultraviolet Resources Intl.. The 510(k) number is K881923.

When did ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72 receive FDA 510(k) clearance?

ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72 received FDA 510(k) clearance on 1988-07-07, under 510(k) number K881923.

Who is the listed applicant for ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72?

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

What is the FDA product code for ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72?

The FDA product code for ULTRAVIOLET RESOURCES INT'L MODEL 2-FS72 is FTC.

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.

Related Devices (Code: FTC)

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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