FGH — Catheter, Double Lumen Female Urethrographic Class II
FDA product code FGH covers "Catheter, Double Lumen Female Urethrographic", a Class II medical device regulated under 21 CFR 876.5130. 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
- FGH
- Device Class
- Class II
- Regulation Number
- 876.5130
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K910196 | c.r. bard | BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS | March 27, 1991 |