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FDA 510(k)

ELECTRIC MOUTH MIRROR

K-Number: K830777 · 1983-04-06

Decision Date1983-04-06
Product CodeEAX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELECTRIC MOUTH MIRROR is the device name listed in this FDA 510(k) record. The listed applicant is Almore Intl., Inc.. It received FDA 510(k) clearance on 1983-04-06 under 510(k) number K830777. The device is classified under product code EAX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC MOUTH MIRROR?

ELECTRIC MOUTH MIRROR is a medical device that received FDA 510(k) clearance on 1983-04-06. The listed applicant is Almore Intl., Inc.. The 510(k) number is K830777.

When did ELECTRIC MOUTH MIRROR receive FDA 510(k) clearance?

ELECTRIC MOUTH MIRROR received FDA 510(k) clearance on 1983-04-06, under 510(k) number K830777.

Who is the listed applicant for ELECTRIC MOUTH MIRROR?

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

What is the FDA product code for ELECTRIC MOUTH MIRROR?

The FDA product code for ELECTRIC MOUTH MIRROR is EAX.

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 Almore Intl., 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.

View all 21 devices →

Related Devices (Code: EAX)

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

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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