ACTIVE VERTICAL CORRECTOR ACTIVE BITE
K-Number: K843344 · 1984-12-03
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Device Summary
Frequently Asked Questions
What is the ACTIVE VERTICAL CORRECTOR ACTIVE BITE?
ACTIVE VERTICAL CORRECTOR ACTIVE BITE is a medical device that received FDA 510(k) clearance on 1984-12-03. The listed applicant is Active Vertical Correctors, Inc.. The 510(k) number is K843344.
When did ACTIVE VERTICAL CORRECTOR ACTIVE BITE receive FDA 510(k) clearance?
ACTIVE VERTICAL CORRECTOR ACTIVE BITE received FDA 510(k) clearance on 1984-12-03, under 510(k) number K843344.
Who is the listed applicant for ACTIVE VERTICAL CORRECTOR ACTIVE BITE?
The FDA 510(k) record lists Active Vertical Correctors, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACTIVE VERTICAL CORRECTOR ACTIVE BITE?
The FDA product code for ACTIVE VERTICAL CORRECTOR ACTIVE BITE is ECO.
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 Active Vertical Correctors, 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: ECO)
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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