# K952141: Sas Francisella Tularensis Antiserum

- Pathway: 510(k) (Traditional)
- Applicant: Sa Scientific, Inc.
- Decided: Jul 21, 1995 after 74 days
- Product code: GSK (Antiserum, Francisella Tularensis)
- Device class: 2
- Regulation: 21 CFR 866.3280
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K072547: Jbaids Tularemia Detection Kit, Model JRPD-Asy-0124 (2007), 1 descendant of its own
- K131936: Jbaids Tularemia Detection Kit (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K952141
Methodology: https://510kreport.com/methodology