EQN
- Product code
- EQN
- Device name
- Laryngoscope, Nasopharyngoscope
- Device class
- Class 2
- 21 CFR
- 21 CFR 874.4760
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 22
FDA classification definition
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K252624 | 2026-05-15 | KARL STORZ Endoscopy-America, Inc. | KARL STORZ Laryngoscopes and Accessories |
Official FDA classification page: EQN
Classification and pathway per current FDA publications. Data from openFDA (CC0).