# K013939: Jostra Flowprobe FP-32E

- Pathway: 510(k) (Traditional)
- Applicant: Jostra AG
- Decided: Dec 14, 2001 after 15 days
- Product code: DPT (Probe, Blood-Flow, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2120
- Recalls of this device: none
- 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. The FDA summary names its predicate without a number.
- (no number) Medtronic-BioMedicus DP-38 Bio-Probe: named in the summary without a submission number

## Indications for use
The Jostra Flowprobe FP-32E is indicated for use as a flow measuring device to be used in conjunction with an electromagnetic blood flow transducer as a direct product substitution for the Medtronic BioMedicus flowprobe DP-38 in extracorporeal circuits for up to 6 hours.

Source page: https://510kreport.com/device/K013939
Methodology: https://510kreport.com/methodology