# K062308: LMT-Kath-S; LMT-Kath-I

- Pathway: 510(k) (Abbreviated)
- Applicant: Licher Medizintechnologie GmbH
- Decided: Mar 20, 2007 after 224 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K003977 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003977: Disetronic Rapid Subcutaneous Infusion Set and Disteronic Rapid D Subcutaneous Infusion Set, Disetronic Medical Systems AG (2001) Summary page 1.

## Indications for use
LMT-KATH-S 28G 10mm x 60cm / 0,394" x 23,62" LMT-KATH-S 28G 8mm x 60cm / 0,315" x 23,62" LMT-KATH-I 25G 12mm x 60cm / 0,472" x 23,62" LMT-KATH-I 25G 8mm x 60cm /0,315" x 23,62" Infusion Sets are indicated for the infusion and/or injection of medication that is dispensed by means of micro-dosage pump into the body below the surface of the skin.

Source page: https://510kreport.com/device/K062308
Methodology: https://510kreport.com/methodology