HFL — Drain, Cervical Class II
FDA product code HFL covers "Drain, Cervical", a Class II medical device regulated under 21 CFR 884.3200. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- HFL
- Device Class
- Class II
- Regulation Number
- 884.3200
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K903989 | sil-med | SIL-MED T-TUBE DRAIN | January 31, 1991 |