# K972206: Nipro Blood Tubing Set with Transducer and Solution Set for Hemodialysis

- Pathway: 510(k) (Traditional)
- Applicant: Nipro Medical Corp.
- Decided: Nov 26, 1997 after 168 days
- Product code: KOC (Accessories, Blood Circuit, Hemodialysis)
- Device class: 2
- Regulation: 21 CFR 876.5820
- 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. The FDA summary names its predicate without a number.
- (no number) Medisystems Corporation ReadySet™ Hemodialysis Blood Tubing Set with Priming Set and Transducer Protectors: named in the summary without a submission number

## Most influential descendants
- K013634: Bioteque 3 in 1 Hemodialysis Blood Tubing Pack (2002), 0 descendants of its own

## Indications for use
The Nipro® Blood Tubing Set for Hemodialysis with Transducer Protectors and Priming Set is intended for use during hemodialysis to provide access to a patient's blood. When used in hemodialysis, they are part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions.

Source page: https://510kreport.com/device/K972206
Methodology: https://510kreport.com/methodology