The following data is part of a premarket notification filed by Acclarent, Inc. with the FDA for Relieva Ultirra Sinus Balloon Catheter.
| Device ID | K190525 |
| 510k Number | K190525 |
| Device Name: | RELIEVA ULTIRRA Sinus Balloon Catheter |
| Classification | Instrument, Ent Manual Surgical |
| Applicant | Acclarent, Inc. 33 Technology Drive Irvine, CA 92618 |
| Contact | Leena Sorathia |
| Correspondent | Leena Sorathia Acclarent, Inc. 33 Technology Drive Irvine, CA 92618 |
| Product Code | LRC |
| CFR Regulation Number | 874.4420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-03-04 |
| Decision Date | 2019-05-03 |