K30000 Dental Chair
FDA 510(k) K822740 · Kaycor Intl., Ltd.
510(k) numberK822740
Submission
- Device name
- K30000 Dental Chair
- Applicant
- Kaycor Intl., Ltd.
Mchenry, IL, US - Received
- September 9, 1982
- Decision date
- September 28, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code KLC
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K233921 | Luvis Chair (LC700C)KLC · Traditional | Dentis Co., Ltd. | 09/06/2024SE |
| K151987 | DCI Edge Dental Chair with Operative UnitKLC · Traditional | Dci | 06/01/2016SE |
| K071353 | Foshion Chair Mounted Dental, Model FJ48CKLC · Traditional | Shanghai Foshion Medical Instruments Co., Ltd. | 12/14/2007SE |
| K971063 | Optima Plus E Dental Chair; a Dental Chair; Excel ChairKLC · Traditional | King Dental Corp. | 06/03/1997SE |
| K963209 | Prostyle CompactKLC · Traditional | Planmeca Oy | 10/24/1996SE |
| K942870 | Ultima 2 Dental ChairKLC · Traditional | Dentech Corp. | 02/27/1995SE |
| K940950 | Kavo Systematica 1060KLC · Traditional | Kavo America | 12/29/1994SE |
| K925567 | E 4000 Dental Operating ChairKLC · Traditional | Dentalez Group | 03/10/1994SE |
| K925119 | A-Dec 1040 ChairKLC · Traditional | A-Dec, Inc. | 01/31/1994SE |
| K923534 | PM2002 ProlineKLC · Traditional | Planmeca USA, Inc. | 01/31/1994SE |
More from Planmeca USA, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K965072 | Panoura Ultra Pan and Panoura Ultra Pan/Ceph Panoramic/Cephalometric X-Ray UnitEHD · Traditional | 01/27/1997SE |
| K931717 | Yoshida/Kaycor X-707 Wall Mounted Dental X-RayEAP · Traditional | 09/20/1993SE |
| K832063 | Robin Cordless HandpieceEKX · Traditional | 08/26/1983SE |
| K813348 | Yoshida Rido-F, Model LM-01EKX · Traditional | 01/07/1982SE |
| K811210 | Yoshida-Panoura 10 · Traditional | 08/24/1981SE |
| K811211 | Yoshida Ap 100EGY · Traditional | 06/16/1981SE |
Questions and answers
When was K30000 Dental Chair cleared by the FDA?
K30000 Dental Chair (K822740) received a 510(k) decision of Substantially Equivalent on September 28, 1982, 19 days after the submission was received.
What is the product code of K822740?
The FDA product code is KLC – Chair, Dental, With Operative Unit, a Class I (low risk) device regulated under 21 CFR 872.6250.