FDA Product Code
FDA Product Code QGK — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ear, Nose, Throat
- 21 CFR Citation
- 874.4420
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K183090 | Relieva Tract Balloon Dilation System | Acclarent, Inc. | 2019-04-19 | Traditional | PDF ↗ |
Product code QGK · Class I · Ear, Nose, Throat. Data: openFDA.