Product code MAJ— Anesthesiology
IPI ALGO-LINE CATHETER
- Classification name
- Catheter, Percutaneous, Intraspinal, Short Term
- Device class
- Class 2
- Regulation
- 21 CFR 868.5120
- Advisory panel
- Anesthesiology
- Total cleared
- 6
- First cleared
- Most recent
Market context for product code MAJ
FDA has cleared devices under product code MAJ between 1989 and 1997, filed by 4 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1997
- 1995
- 1993
- 1991
- 1989
Top applicants under product code MAJ
Recent clearances under product code MAJ
- K965251 — MEDTRONIC ALGOLINE INTRASPINAL CATHETER SYSTEM
- K934939 — TEMPORARY SCREENING LEAD/ CATHETER KIT
- K945413 — MEDTRONIC MODEL 3864C & 3865C TEMPORARY SCREENING LEAD/CATHETER KIT
- K930218 — SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
- K911382 — IPI ALGO-LINE CATHETER
- K893766 — LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE
Data sourced from openFDA. This site is unofficial and independent of the FDA.