Dental Chair, Vanguard

FDA 510(k) K772300 · Ritter Co.

Substantially Equivalent

510(k) numberK772300

Submission

Device name
Dental Chair, Vanguard
Applicant
Ritter Co.
Mchenry, IL, US
Received
December 14, 1977
Decision date
January 3, 1978
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

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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
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More from Planmeca USA, Inc.

510(k)DeviceDecision
K831245Taylor Printer/Auto Inflat-SphygmomanoDXN · Traditional 10/19/1983SE
K832171Self Check Digital Blood Press. MonitorDXN · Traditional 10/04/1983SE
K831976Power OpticEAY · Traditional 08/12/1983SE
K823180SA-21 Dental UnitEIA · Traditional 11/22/1982SE
K800084Ritter Model J Dental ChairKLC · Traditional 01/29/1980SE
K781101Electrosurgical Unit 75GEI · Traditional 07/17/1978SE
K780293Electrosurgical UnitHAM · Traditional 03/14/1978SE
K760929Accutorq IIEFB · Traditional 11/19/1976SE
K760707Ritter Starlight Dental Operating LightEAZ · Traditional 10/05/1976SE

Questions and answers

When was Dental Chair, Vanguard cleared by the FDA?

Dental Chair, Vanguard (K772300) received a 510(k) decision of Substantially Equivalent on January 3, 1978, 20 days after the submission was received.

What is the product code of K772300?

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