FIW
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Alarm, Pillow Pressure
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5820
- Medical specialty
- Gastroenterology, Urology
- Flags
- Life-sustaining
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| Record | Firm | Date | Builder |
|---|---|---|---|
| BLOOD LINE COMP. NEG. PRESS. PILLOW (K772355) | Cordis Corp. | 1978-01-26 | + Add |
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Every clearance here is in the API, with alerts when new ones post.