The following data is part of a premarket notification filed by Xomed, Inc. with the FDA for Maxill-air Sinus Ventilation Tube.
| Device ID | K813474 |
| 510k Number | K813474 |
| Device Name: | MAXILL-AIR SINUS VENTILATION TUBE |
| Classification | Cannula, Sinus |
| Applicant | XOMED, INC. 1318 LONEDELL RD. Arnold, MO 63010 |
| Product Code | KAM |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-01 |
| Decision Date | 1982-01-12 |