# K871080: Peripherally Inserted Central Venous Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Catheter Technology Corp.
- Decided: Aug 12, 1987 after 147 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Aug 8, 2014 · Class II · Z-1275-2015: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit open seals, which could impact product sterility. Bard includes these pouched syringes, attached to some configurations of 

Source page: https://510kreport.com/device/K871080
Methodology: https://510kreport.com/methodology