# K912660: Securodrip

- Pathway: 510(k) (Traditional)
- Applicant: Op-Co Medical Products, Ltd.
- Decided: Dec 4, 1991 after 170 days
- Product code: KMK (Device, Intravascular Catheter Securement)
- Device class: 1
- Regulation: 21 CFR 880.5210
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Source page: https://510kreport.com/device/K912660
Methodology: https://510kreport.com/methodology