# K070143: JMS Planecta Stopcock

- Pathway: 510(k) (Traditional)
- Applicant: Jms North America Corp.
- Decided: Apr 10, 2007 after 84 days
- Product code: FMG (Stopcock, I.V. Set)
- 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 K974083 (1998). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023668: JMS Extension Set with Planecta, Planecta (Stand Alone Unit), Planecta Lock & Planecta Adaptor, Jms North America Corp. (2003) Summary page 2.
- K974083: Connecta Plus 1 and Connecta Plus 3 2-Way and 3-Way Stopcocks, Ohmeda Medical (1998) Summary page 2.

## Indications for use
JMS Planecta® Stopcock (PNSC) is indicated for fluid flow directional control and for providing access port(s) for administration of solutions, withdrawal of fluids and pressure monitoring. JMS Planecta® Stopcock can be used by itself, or as component to administration/extension set, and aids in the prevention of needle stick injuries.

Source page: https://510kreport.com/device/K070143
Methodology: https://510kreport.com/methodology