# K943472: Cohort Avb Retractor System

- Pathway: 510(k) (Traditional)
- Applicant: Cohort Medical Products Group, Inc.
- Decided: Oct 20, 1994 after 93 days
- Product code: HXB (Probe)
- Device class: 1
- Regulation: 21 CFR 888.4540
- Recalls of this device: none
- 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.

Source page: https://510kreport.com/device/K943472
Methodology: https://510kreport.com/methodology