Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR

K-Number: K971063 · 1997-06-03

Decision Date1997-06-03
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is King Dental Corp.. It received FDA 510(k) clearance on 1997-06-03 under 510(k) number K971063. 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 OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR?

OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR is a medical device that received FDA 510(k) clearance on 1997-06-03. The listed applicant is King Dental Corp.. The 510(k) number is K971063.

When did OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR receive FDA 510(k) clearance?

OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR received FDA 510(k) clearance on 1997-06-03, under 510(k) number K971063.

Who is the listed applicant for OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR?

The FDA 510(k) record lists King Dental Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR?

The FDA product code for OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL 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 King Dental Corp. 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑