Product code
KNH: Laparoscopic contraceptive tubal occlusion device
FDA product code · Class III · Obstetrics/Gynecology
Key facts
| Product code | KNH |
|---|---|
| Device | Laparoscopic contraceptive tubal occlusion device |
| Device class | Class III |
| Regulation number | 884.5380 |
| Review panel | Obstetrics/Gynecology |
| Medical specialty | Obstetrics/Gynecology |
| Submission type | PMA |
| GMP exempt | No |
| Implanted device | Yes |
| Life-sustaining or life-supporting | No |
| Definition | Call for PMAs to be filed by 12/30/87 (52 FR 36883 (10/1/87)) |
At a glance
- None 510(k) clearances
- None De Novo grants
- 1–9 PMA approvals
- None HDE approvals
- 10–99 UDI devices (GUDID)
- 1,000+ MAUDE adverse event reports
- 1–9 Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database