LLD — Port & Catheter, Implanted, Subcutaneous, Intraperitoneal Class II
FDA product code LLD covers "Port & Catheter, Implanted, Subcutaneous, Intraperitoneal", a Class II medical device regulated under 21 CFR 880.5965. Submissions are reviewed by the General Hospital panel. Devices under this code are implants. At least 4 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- LLD
- Device Class
- Class II
- Regulation Number
- 880.5965
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K880072 | pharmacia deltec | PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM | March 29, 1988 |
| K864552 | pharmacia | PORT-A-CATH IMPLANTABLE CATHETER SYSTEM | March 31, 1987 |
| K862412 | burron medical products | INTESTOPLANT | November 13, 1986 |
| K832906 | pharmacia | PORT-A-CATH IMPLANTABLE CATHETER SYS | March 6, 1984 |