Dental Chairs

FDA 510(k) K760599 · Chayes Virginia, Inc.

Substantially Equivalent

510(k) numberK760599

Submission

Device name
Dental Chairs
Applicant
Chayes Virginia, Inc.
Mchenry, IL, US
Received
September 7, 1976
Decision date
September 15, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KLC – Chair, Dental, With Operative Unit
Device class
Class I (low risk)
Regulation
21 CFR 872.6250
Specialty
Dental

Other 510(k)s with product code KLC

510(k)DeviceApplicantDecision
K233921Luvis Chair (LC700C)KLC · Traditional Dentis Co., Ltd.09/06/2024SE
K151987DCI Edge Dental Chair with Operative UnitKLC · Traditional Dci06/01/2016SE
K071353Foshion Chair Mounted Dental, Model FJ48CKLC · Traditional Shanghai Foshion Medical Instruments Co., Ltd.12/14/2007SE
K971063Optima Plus E Dental Chair; a Dental Chair; Excel ChairKLC · Traditional King Dental Corp.06/03/1997SE
K963209Prostyle CompactKLC · Traditional Planmeca Oy10/24/1996SE
K942870Ultima 2 Dental ChairKLC · Traditional Dentech Corp.02/27/1995SE
K940950Kavo Systematica 1060KLC · Traditional Kavo America12/29/1994SE
K925567E 4000 Dental Operating ChairKLC · Traditional Dentalez Group03/10/1994SE
K925119A-Dec 1040 ChairKLC · Traditional A-Dec, Inc.01/31/1994SE
K923534PM2002 ProlineKLC · Traditional Planmeca USA, Inc.01/31/1994SE

More from Planmeca USA, Inc.

510(k)DeviceDecision
K820907DentiscopeEAY · Traditional 05/05/1982SE
K771873Vision Series Dental ChairKLC · Traditional 10/25/1977SE
K771890Perception Series Delivery Sys.EIA · Traditional 10/20/1977SE

Questions and answers

When was Dental Chairs cleared by the FDA?

Dental Chairs (K760599) received a 510(k) decision of Substantially Equivalent on September 15, 1976, 8 days after the submission was received.

What is the product code of K760599?

The FDA product code is KLC – Chair, Dental, With Operative Unit, a Class I (low risk) device regulated under 21 CFR 872.6250.