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FDA 510(k)

E 4000 DENTAL OPERATING CHAIR

K-Number: K925567 · 1994-03-10

Decision Date1994-03-10
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

E 4000 DENTAL OPERATING CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Dentalez Group. It received FDA 510(k) clearance on 1994-03-10 under 510(k) number K925567. 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 E 4000 DENTAL OPERATING CHAIR?

E 4000 DENTAL OPERATING CHAIR is a medical device that received FDA 510(k) clearance on 1994-03-10. The listed applicant is Dentalez Group. The 510(k) number is K925567.

When did E 4000 DENTAL OPERATING CHAIR receive FDA 510(k) clearance?

E 4000 DENTAL OPERATING CHAIR received FDA 510(k) clearance on 1994-03-10, under 510(k) number K925567.

Who is the listed applicant for E 4000 DENTAL OPERATING CHAIR?

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

What is the FDA product code for E 4000 DENTAL OPERATING CHAIR?

The FDA product code for E 4000 DENTAL OPERATING 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 Dentalez Group 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 13 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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