# K010264: Nipro Blood Tubing Set for Hemodialysis with Transducer Protectors and Priming Set

- Pathway: 510(k) (Traditional)
- Applicant: Nipro Medical Corp.
- Decided: Apr 27, 2001 after 88 days
- Product code: FIB (Protector, Transducer, Dialysis)
- 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.
31 later devices descend from it; 2 cite it directly.
0 of 32 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
- K072024: Nipro Blood Tubing Set with Transducer Protector and Priming Set, Model A201-A219, V801-V806, 5M9634, 5M9693 (2007), 16 descendants of its own
- K082719: Nikkline Blood Tubing Lines with Transducer Protectors, Models AV06A-P, AVO6B-P, AV06C-P (2009), 13 descendants of its own
- K120823: BVM Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors (2012), 8 descendants of its own
- K140841: Tablo Cartridge (2014), 7 descendants of its own
- K112314: Nephros Olpur H2H Hemodiafiltration (HDF) Module and Olpur MD 220 Hemodiafilter (2012), 5 descendants of its own

Source page: https://510kreport.com/device/K010264
Methodology: https://510kreport.com/methodology