DQB
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Phlebograph, Impedance
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2750
- Medical specialty
- Cardiovascular
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| VASOSCREEN IMPEDANCE PLETHYSMOGRAPH (K851102) | Sonicaid, Inc. | 1985-05-16 |
| DEVETHERM (K822873) | Eko Scann AB | 1983-03-24 |
| IMPEDANCE RHEOGRAPH (K772093) | Dynatech Research & Development Co. | 1977-11-18 |
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Every clearance here is in the API, with alerts when new ones post.