FDA Product Code
FDA Product Code LQK — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Obstetrics/Gynecology
- 21 CFR Citation
- 884.2730
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K253673 | Mcare System (MW-20) | Marani Health, Inc. | 2026-09-03 | Traditional | PDF ↗ |
| K221046 | Invu by Nuvo | Nuvo- Group , Ltd. | 2022-05-06 | Special | PDF ↗ |
| K210025 | INVU by Nuvo | Nuvo- Group , Ltd. | 2021-05-28 | Traditional | PDF ↗ |
| K191401 | PregSense | Nuvo- Group , Ltd. | 2020-03-27 | Traditional | PDF ↗ |
| K143114 | Sense4Baby System Model B+ (MSA) | Airstrip Technologies, Inc. | 2015-03-10 | Traditional | PDF ↗ |
| K020390 | MODIFICATION TO FETAL ASSIST | Huntleigh Diagnostics , Ltd. | 2002-04-19 | Traditional | PDF ↗ |
Product code LQK · Class II · Obstetrics/Gynecology. Data: openFDA.