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FDA 510(k)

LOGOS JUNIOR DENTAL CHAIR AND UNIT

K-Number: K023513 · 2003-03-26

Decision Date2003-03-26
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOGOS JUNIOR DENTAL CHAIR AND UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Castellini S.P.A.. It received FDA 510(k) clearance on 2003-03-26 under 510(k) number K023513. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOGOS JUNIOR DENTAL CHAIR AND UNIT?

LOGOS JUNIOR DENTAL CHAIR AND UNIT is a medical device that received FDA 510(k) clearance on 2003-03-26. The listed applicant is Castellini S.P.A.. The 510(k) number is K023513.

When did LOGOS JUNIOR DENTAL CHAIR AND UNIT receive FDA 510(k) clearance?

LOGOS JUNIOR DENTAL CHAIR AND UNIT received FDA 510(k) clearance on 2003-03-26, under 510(k) number K023513.

Who is the listed applicant for LOGOS JUNIOR DENTAL CHAIR AND UNIT?

The FDA 510(k) record lists Castellini S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOGOS JUNIOR DENTAL CHAIR AND UNIT?

The FDA product code for LOGOS JUNIOR DENTAL CHAIR AND UNIT is EIA.

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 Castellini S.P.A. 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: EIA)

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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