# K063469: Medican Alpha

- Pathway: 510(k) (Traditional)
- Applicant: Eastern Medikit, Ltd.
- Decided: Dec 1, 2006 after 15 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: 2 generations back to K801941 (1980). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982805: Introcan Safety IV Catheter, B.Braun Medical, Inc. (1999) Summary page 1.
- K013073: Insyte, Angiocath, Insyte Autoguard, Angiocath Autoguard, Autoguard Pro, Intima and Saf-T-Intima Intravascular Catheters, Becton Dickinson Infusion Therapy Systems, Inc. (2001) Summary page 1.

## Indications for use
Infusion of I.V. Solutions, Intermittent intravenous Drug administration.

Source page: https://510kreport.com/device/K063469
Methodology: https://510kreport.com/methodology