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FDA 510(k)

VISION SERIES DENTAL CHAIR

K-Number: K771873 · 1977-10-25

Decision Date1977-10-25
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VISION SERIES DENTAL CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Chayes Virginia, Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771873. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISION SERIES DENTAL CHAIR?

VISION SERIES DENTAL CHAIR is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Chayes Virginia, Inc.. The 510(k) number is K771873.

When did VISION SERIES DENTAL CHAIR receive FDA 510(k) clearance?

VISION SERIES DENTAL CHAIR received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771873.

Who is the listed applicant for VISION SERIES DENTAL CHAIR?

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

What is the FDA product code for VISION SERIES DENTAL CHAIR?

The FDA product code for VISION SERIES DENTAL CHAIR is KLC.

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 Chayes Virginia, 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: KLC)

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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