# K913861: Hemochron (R) Kact

- Pathway: 510(k) (Traditional)
- Applicant: International Technidyne Corp.
- Decided: Oct 18, 1991 after 52 days
- Product code: JBP (Activated Whole Blood Clotting Time)
- Device class: 2
- Regulation: 21 CFR 864.7140
- 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; 2 cite 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
- K992851: Act Test Catridges for Coaguchek Pro System, Act Controls for Coaguchek Pro System (2000), 0 descendants of its own
- K971935: B&D Activated Clotting Time (Act) Test Tubes BD-C101 (Diatomaceous Earth) and BD-K101 (Kaolin) (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K913861
Methodology: https://510kreport.com/methodology