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FDA 510(k)

IMPROVED DENTAL CHAIR

K-Number: K920016 · 1992-03-02

Decision Date1992-03-02
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPROVED DENTAL CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. It received FDA 510(k) clearance on 1992-03-02 under 510(k) number K920016. 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 IMPROVED DENTAL CHAIR?

IMPROVED DENTAL CHAIR is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. The 510(k) number is K920016.

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

IMPROVED DENTAL CHAIR received FDA 510(k) clearance on 1992-03-02, under 510(k) number K920016.

Who is the listed applicant for IMPROVED DENTAL CHAIR?

The FDA 510(k) record lists Den-Tal-Ez Mfg Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPROVED DENTAL CHAIR?

The FDA product code for IMPROVED 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 Den-Tal-Ez Mfg Co., 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 7 devices →

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

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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