# K896546: Homepump (Disp. Elastomeric Infusion Device)

- Pathway: 510(k) (Traditional)
- Applicant: Block Medical, Inc.
- Decided: Feb 6, 1990 after 81 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K060258: Autofuser (2006), 1 descendant of its own
- K971362: Personal Infusor (1997), 1 descendant of its own
- K090300: Modification to Autofuser (2009), 0 descendants of its own
- K052817: Eureka Infusion Pump, Models Eureka-IP, Eureka-LF (2006), 0 descendants of its own
- K990208: Personal Infusor with Drug Disposal Septal Port (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K896546
Methodology: https://510kreport.com/methodology