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FDA 510(k)

THE GNATHOMETER-M

K-Number: K810972 · 1981-05-05

Decision Date1981-05-05
Product CodeKZO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE GNATHOMETER-M is the device name listed in this FDA 510(k) record. The listed applicant is Bauer, Cheng & Associates, Inc.. It received FDA 510(k) clearance on 1981-05-05 under 510(k) number K810972. The device is classified under product code KZO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 11 devices →

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

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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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