The following data is part of a premarket notification filed by Kaycor Intl., Ltd. with the FDA for K30000 Dental Chair.
| Device ID | K822740 |
| 510k Number | K822740 |
| Device Name: | K30000 DENTAL CHAIR |
| Classification | Chair, Dental, With Operative Unit |
| Applicant | KAYCOR INTL., LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KLC |
| CFR Regulation Number | 872.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-09-09 |
| Decision Date | 1982-09-28 |