# K926204: Sas One Step Pregnancy

- Pathway: 510(k) (Traditional)
- Applicant: Sa Scientific, Inc.
- Decided: Feb 2, 1993 after 55 days
- Product code: JHI (Visual, Pregnancy Hcg, Prescription Use)
- Device class: 2
- Regulation: 21 CFR 862.1155
- 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; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K983090: Acon Midstream Pregnancy Test (1998), 4 descendants of its own
- K050546: Acon +/- Midstream Pregnancy Test (2005), 0 descendants of its own
- K042151: Acon Spectrum HCG Midstream Pregnancy Test (2004), 0 descendants of its own
- K032510: Acon Quik-Check II Midstream Home Pregnancy Test (2003), 0 descendants of its own
- K023037: Mid Stream Pregnancy Test (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K926204
Methodology: https://510kreport.com/methodology