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FDA 510(k)

MOUTH PROPS

K-Number: K940785 · 1994-10-05

Decision Date1994-10-05
Product CodeEIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MOUTH PROPS is the device name listed in this FDA 510(k) record. The listed applicant is Worldwide Dental, Inc.. It received FDA 510(k) clearance on 1994-10-05 under 510(k) number K940785. The device is classified under product code EIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOUTH PROPS?

MOUTH PROPS is a medical device that received FDA 510(k) clearance on 1994-10-05. The listed applicant is Worldwide Dental, Inc.. The 510(k) number is K940785.

When did MOUTH PROPS receive FDA 510(k) clearance?

MOUTH PROPS received FDA 510(k) clearance on 1994-10-05, under 510(k) number K940785.

Who is the listed applicant for MOUTH PROPS?

The FDA 510(k) record lists Worldwide Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOUTH PROPS?

The FDA product code for MOUTH PROPS is EIF.

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 Worldwide Dental, Inc. 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: EIF)

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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