# K001795: The Avitro LLC, 10 and 100 Uso Units/ML Heparin Sodium Vafd

- Pathway: 510(k) (Traditional)
- Applicant: Avitro, LLC
- Decided: Oct 19, 2000 after 127 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K092938: Heparin Lock Flush Solution Usp, Models 504401, 504411, 504505, 505701, 504901, 1710 (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K001795
Methodology: https://510kreport.com/methodology