# K974543: L-Cath Modified Seldinger Technique Insertion/Catheter Exchange Kit PE-MST24-24 GA. Kit, L-Cath Modified Seldinger

- Pathway: 510(k) (Traditional)
- Applicant: Luther Medical Products, Inc.
- Decided: Feb 10, 1998 after 69 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Arrow International MST Kit: named in the summary without a submission number
- (no number) HDC Corporation MST Kit: named in the summary without a submission number
- (no number) Cook Critical Care MST Kit: named in the summary without a submission number

## Indications for use
The L-Cath Modified Seldinger Technique Accessory Kit is designed for placement and/or exchange of the L-Cath Peripherally Inserted Catheter System in 16 ga. (5Fr.), 18 ga. (4Fr.), 20 ga. (3Fr.), 24 ga. (2.6 Fr.) and the L-Cath Dual Lumen 16 and 18 ga. Utilization of a Modified Seldinger Technique for catheter placement has been demonstrated to be effective for the placement of peripherally inserted central catheters in patients, pediatric and adult, with difficult to access veins.

Source page: https://510kreport.com/device/K974543
Methodology: https://510kreport.com/methodology