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FDA 510(k)

THE WOOG ORATEST

K-Number: K874374 · 1988-01-19

ApplicantWoog Intl.
Decision Date1988-01-19
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE WOOG ORATEST is the device name listed in this FDA 510(k) record. The listed applicant is Woog Intl.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K874374. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE WOOG ORATEST?

THE WOOG ORATEST is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Woog Intl.. The 510(k) number is K874374.

When did THE WOOG ORATEST receive FDA 510(k) clearance?

THE WOOG ORATEST received FDA 510(k) clearance on 1988-01-19, under 510(k) number K874374.

Who is the listed applicant for THE WOOG ORATEST?

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

What is the FDA product code for THE WOOG ORATEST?

The FDA product code for THE WOOG ORATEST is EAZ.

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 Woog Intl. 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.

K871406THE WOOG ORABRUSH

Related Devices (Code: EAZ)

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.

K072309MICROLUX/BLUAddent, Inc.K041614MICROLUX DLAddent, Inc.K033033VIZILITE-BLUE ORAL EXAM KITTrylon Corp.K003995SPECULITE/ORALLITETrylon Corp.K926081DENTAL LIGHTMdt Corp., Inc.K935390SIROLUX FANTASTICPelton & Crane Co.

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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