The following data is part of a premarket notification filed by Steven Lamberg, D.d.s with the FDA for Laimad.
| Device ID | K062333 |
| 510k Number | K062333 |
| Device Name: | LAIMAD |
| Classification | Device, Anti-snoring |
| Applicant | STEVEN LAMBERG, D.D.S 555 THIRTEEN STREET, NW Washington, DC 20004 -1109 |
| Contact | Jonathan S Kahan |
| Correspondent | Jonathan S Kahan STEVEN LAMBERG, D.D.S 555 THIRTEEN STREET, NW Washington, DC 20004 -1109 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-10 |
| Decision Date | 2006-12-14 |
| Summary: | summary |