# K830256: Non-Sterile Broviac Parenteral Alimi-

- Pathway: 510(k) (Traditional)
- Applicant: Evermed, Inc.
- Decided: Mar 1, 1983 after 35 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- 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.
128 later devices descend from it; 1 cites it directly.
15 of 129 devices 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.

## Most influential descendants
- K050185: Powerhohn and Powerline Catheters (2005), 127 descendants of its own
- K051417: 6 FR FL Powerhohn and Powerline Catheter (2005), 126 descendants of its own
- K051991: Powerpicc, Poly Per-Q-Cath, 6 FR TL Poly Per-Q-Cath, Power Hohn and Power Line (2005), 119 descendants of its own
- K070996: 4 FR Single Lumen (SL) Powerpicc Catheter (2007), 66 descendants of its own
- K061179: Powerhickman Long-Term Intravascular Catheter (2006), 47 descendants of its own

## Recalls of this device
- Dec 12, 2025 · Class II · Z-1367-2026: Due to damage to outer tray that can potentially compromise the sterile barrier

Source page: https://510kreport.com/device/K830256
Methodology: https://510kreport.com/methodology