HGW
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Sampler, Blood, Fetal
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.1560
- Medical specialty
- Obstetrics/Gynecology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| 1570 - FETAL BLOOD SAMPLING KIT (K891388) | Transidyne General Corp. | 1989-03-28 |
| ROCKET FETAL BLOOD SAMPLING TRAY (K884685) | A & A Medical, Inc. | 1989-01-12 |
| FETAL BLOOD SAMPLING KIT #1560 (K831459) | Transidyne General Corp. | 1983-06-30 |
| FETAL BLOOD SAMPLING KIT MODEL 1560 (K810028) | Transidyne General Corp. | 1981-01-16 |
Track HGW automatically
Every clearance here is in the API, with alerts when new ones post.