FDA Product Code
FDA Product Code KXP — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Obstetrics/Gynecology
- 21 CFR Citation
- 884.3900
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K202542 | Allura Vaginal Stent | Pmt Corporation | 2020-09-30 | Traditional | PDF ↗ |
| K983045 | AMIELLE | Owen Mumford USA, Inc. | 1998-11-25 | Traditional | PDF ↗ |
| K974479 | SILIMED VAGINAL STENT | Silimed, LLC | 1998-08-05 | Traditional | PDF ↗ |
| K920633 | PESSARY FLEXIBLE SILICONE NICHOLS | Bioteque America, Inc. | 1995-11-08 | Traditional | PDF ↗ |
Product code KXP · Class II · Obstetrics/Gynecology. Data: openFDA.