FDA 510(k)

K30000 DENTAL CHAIR

K-Number: K822740 · 1982-09-28

Decision Date1982-09-28

Product CodeKLC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

K30000 DENTAL CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Kaycor Intl., Ltd.. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K822740. 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 K30000 DENTAL CHAIR?

K30000 DENTAL CHAIR is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Kaycor Intl., Ltd.. The 510(k) number is K822740.

When did K30000 DENTAL CHAIR receive FDA 510(k) clearance?

K30000 DENTAL CHAIR received FDA 510(k) clearance on 1982-09-28, under 510(k) number K822740.

Who is the listed applicant for K30000 DENTAL CHAIR?

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

What is the FDA product code for K30000 DENTAL CHAIR?

The FDA product code for K30000 DENTAL CHAIR is KLC.

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Other records listing Kaycor Intl., Ltd. as applicant

K965072PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT K931717YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY K832063ROBIN CORDLESS HANDPIECE K813348YOSHIDA RIDO-F, MODEL LM-01 K811210YOSHIDA-PANOURA 10 K811211YOSHIDA AP 100

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Related Devices (Code: KLC)

K233921Luvis Chair (LC700C)Dentis Co., Ltd.K151987DCI Edge Dental Chair with Operative UnitDci K071353FOSHION CHAIR MOUNTED DENTAL, MODEL FJ48CShanghai Foshion Medical Instruments Co., Ltd.K971063OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIRKing Dental Corp.K963209PROSTYLE COMPACTPlanmeca Oy K942870ULTIMA 2 DENTAL CHAIRDentech Corp.

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.