KOH
- Product code
- KOH
- Device name
- Instrument, Manual, General Obstetric-Gynecologic
- Device class
- Class 1
- 21 CFR
- 21 CFR 884.4520
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 15 (all years; only the last 3 years are listed here)
Official FDA classification page: KOH
Classification and pathway per current FDA publications. Data from openFDA (CC0).