LRC
- Product code
- LRC
- Device name
- Instrument, Ent Manual Surgical
- Device class
- Class 1
- 21 CFR
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 65 (all years; only the last 3 years are listed here)
Official FDA classification page: LRC
Classification and pathway per current FDA publications. Data from openFDA (CC0).