The following data is part of a premarket notification filed by Luneau Gynecologie Sa with the FDA for L720 Examination Chair.
| Device ID | K001261 |
| 510k Number | K001261 |
| Device Name: | L720 EXAMINATION CHAIR |
| Classification | Table, Obstetric (and Accessories) |
| Applicant | LUNEAU GYNECOLOGIE SA BP 252 Chartres Cedex, FR 28005 |
| Contact | Bernard Hoel |
| Correspondent | Bernard Hoel LUNEAU GYNECOLOGIE SA BP 252 Chartres Cedex, FR 28005 |
| Product Code | KNC |
| CFR Regulation Number | 884.4900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-04-19 |
| Decision Date | 2000-06-08 |