# K910238: Portable Auto Transfusion System 500

- Pathway: 510(k) (Traditional)
- Applicant: Electromedics, Inc.
- Decided: Jun 19, 1991 after 152 days
- Product code: CAC (Apparatus, Autotransfusion)
- Device class: 2
- Regulation: 21 CFR 868.5830
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 3 cite it directly.
0 of 5 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
- K992723: Orthopedic Perioperative Autotransfusion (Orthopat) System (1999), 1 descendant of its own
- K122262: Orthopat Advance Perioperative Autotransfusion System (2012), 0 descendants of its own
- K982660: Orthopedic Perioperative Autotransfusion (Orthopat) System (1999), 0 descendants of its own
- K962475: Orthopedic Perioperative Autotransfusion (Orthopat) System (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K910238
Methodology: https://510kreport.com/methodology