# K932093: Autovac Closed Wound Autotransfusion System,7920 S

- Pathway: 510(k) (Traditional)
- Applicant: Boehringer Laboratories
- Decided: Jul 6, 1994 after 432 days
- Product code: CAC (Apparatus, Autotransfusion)
- Device class: 2
- Regulation: 21 CFR 868.5830
- Recalls of this device: 1 (0 Class I)
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Recalls of this device
- Nov 7, 2003 · Not classified · Z-0227-04: Inadequate bond where the tube attaches to the inlet of the bulb.

Source page: https://510kreport.com/device/K932093
Methodology: https://510kreport.com/methodology