FDA 510(k)

RITTER MODEL J DENTAL CHAIR

K-Number: K800084 · 1980-01-29

Decision Date1980-01-29

Product CodeKLC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

RITTER MODEL J DENTAL CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Ritter Co.. It received FDA 510(k) clearance on 1980-01-29 under 510(k) number K800084. 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 RITTER MODEL J DENTAL CHAIR?

RITTER MODEL J DENTAL CHAIR is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is Ritter Co.. The 510(k) number is K800084.

When did RITTER MODEL J DENTAL CHAIR receive FDA 510(k) clearance?

RITTER MODEL J DENTAL CHAIR received FDA 510(k) clearance on 1980-01-29, under 510(k) number K800084.

Who is the listed applicant for RITTER MODEL J DENTAL CHAIR?

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

What is the FDA product code for RITTER MODEL J DENTAL CHAIR?

The FDA product code for RITTER MODEL J DENTAL CHAIR is KLC.

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Other records listing Ritter Co. as applicant

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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.