THE GNATHOMETER-M
K-Number: K810972 · 1981-05-05
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Device Summary
Frequently Asked Questions
What is the THE GNATHOMETER-M?
THE GNATHOMETER-M is a medical device that received FDA 510(k) clearance on 1981-05-05. The listed applicant is Bauer, Cheng & Associates, Inc.. The 510(k) number is K810972.
When did THE GNATHOMETER-M receive FDA 510(k) clearance?
THE GNATHOMETER-M received FDA 510(k) clearance on 1981-05-05, under 510(k) number K810972.
Who is the listed applicant for THE GNATHOMETER-M?
The FDA 510(k) record lists Bauer, Cheng & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE GNATHOMETER-M?
The FDA product code for THE GNATHOMETER-M is KZO.
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 Bauer, Cheng & Associates, 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: KZO)
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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