FDA 510(k)

DCI Edge Dental Chair with Operative Unit

K-Number: K151987 · 2016-06-01

ApplicantDci

Decision Date2016-06-01

Product CodeKLC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DCI Edge Dental Chair with Operative Unit is the device name listed in this FDA 510(k) record. The listed applicant is Dci. It received FDA 510(k) clearance on 2016-06-01 under 510(k) number K151987. 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 DCI Edge Dental Chair with Operative Unit?

DCI Edge Dental Chair with Operative Unit is a medical device that received FDA 510(k) clearance on 2016-06-01. The listed applicant is Dci. The 510(k) number is K151987.

When did DCI Edge Dental Chair with Operative Unit receive FDA 510(k) clearance?

DCI Edge Dental Chair with Operative Unit received FDA 510(k) clearance on 2016-06-01, under 510(k) number K151987.

Who is the listed applicant for DCI Edge Dental Chair with Operative Unit?

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

What is the FDA product code for DCI Edge Dental Chair with Operative Unit?

The FDA product code for DCI Edge Dental Chair with Operative Unit is KLC.

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.

K233921Luvis Chair (LC700C)Dentis Co., Ltd.

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.