# K885281: Vamp Venous/Arterial Blood Management Protection

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Mar 3, 1989 after 66 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- 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.
9 later devices descend from it; 4 cite it directly.
0 of 10 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
- K161962: VAMP Venous/Arterial Blood Management Protection System (2016), 3 descendants of its own
- K163172: HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer Kit (2017), 2 descendants of its own
- K173586: VAMP Venous/Arterial Blood Management Protection System (2018), 1 descendant of its own
- K172458: HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer Kit (2017), 1 descendant of its own
- K221782: Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes (2023), 0 descendants of its own

## Recalls of this device
- Mar 14, 2008 · Not classified · Z-1934-2009: Edwards Lifescience initiated a recall of on Edwards "VAMP Jr" Pressure Monitoring Products manufactured between 8/01/06 and 2/29/08 due to the potential for the cap on the reservoir of the "VAMP Jr" 

Source page: https://510kreport.com/device/K885281
Methodology: https://510kreport.com/methodology