Sunrise
FDA 510(k) clearance K250874 · decided 2025-08-29
Clearance details
- K-number
- K250874
- Device name
- Sunrise
- Applicant
- Sunrise SA
- Decision
- Substantially Equivalent
- Date received
- 2025-03-24
- Decision date
- 2025-08-29
- Days to decision
- 158 days
- Clearance type
- Traditional
- Product code
- QRS
- Device class
- 2
- Regulation number
- 868.2376
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Namur, BE
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Sunrise SA
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Sunrise (K222262) | Sunrise SA | 2022-12-22 |
| Sunrise Sleep Disorder Diagnostic Aid (DEN210015) | Sunrise | 2022-01-07 |
Recalls involving this device
No recalls on record reference this clearance.