# K951620: Midmark Midline Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Menlo Care, Inc.
- Decided: Apr 4, 1996 after 363 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
Longest line of descent: 1 generation back to K924968 (1993). 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)
- K924968: L-Cath Peel-Away Catheter System, Luther Medical Products, Inc. (1993) Summary page 1.
- (no number) V-Cath® ML: named in the summary without a submission number

## Indications for use
Peripherally inserted catheter for venous access or intravenous therapy.

Source page: https://510kreport.com/device/K951620
Methodology: https://510kreport.com/methodology