MAJ — Catheter, Percutaneous, Intraspinal, Short Term Class II
FDA Device Classification
Classification Details
- Product Code
- MAJ
- Device Class
- Class II
- Regulation Number
- 868.5120
- Submission Type
- Review Panel
- HO
- Medical Specialty
- Anesthesiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K965251 | medtronic vascular | MEDTRONIC ALGOLINE INTRASPINAL CATHETER SYSTEM | March 18, 1997 |
| K945413 | medtronic vascular | MEDTRONIC MODEL 3864C & 3865C TEMPORARY SCREENING LEAD/CATHETER KIT | May 24, 1995 |
| K934939 | medtronic vascular | TEMPORARY SCREENING LEAD/ CATHETER KIT | May 24, 1995 |
| K930218 | concord/portex | SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES | July 27, 1993 |
| K911382 | pudenz-schulte medical research | IPI ALGO-LINE CATHETER | July 18, 1991 |
| K893766 | abbott laboratories | LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE | November 1, 1989 |