FIW — Alarm, Pillow Pressure Class II
FDA product code FIW covers "Alarm, Pillow Pressure", a Class II medical device regulated under 21 CFR 876.5820. Submissions are reviewed by the Gastroenterology, Urology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- FIW
- Device Class
- Class II
- Regulation Number
- 876.5820
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K772355 | cordis | BLOOD LINE COMP. NEG. PRESS. PILLOW | January 26, 1978 |