# K926551: Behring Fibrintimer a

- Pathway: 510(k) (Traditional)
- Applicant: Behring Diagnostics, Inc.
- Decided: Apr 18, 1995 after 838 days
- Product code: JPA (System, Multipurpose For In Vitro Coagulation Studies)
- Device class: 2
- Regulation: 21 CFR 864.5425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 3 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K955278: Behring Coagulation Timer (1996), 10 descendants of its own
- K992321: Sysmex Automated Coagulation Analyzer, Model CA-6000 (1999), 4 descendants of its own
- K993174: Sysmex Automated Coagulation Analyzer, Model CA-6000 (1999), 2 descendants of its own
- K970431: Behring Coagulation System (1997), 2 descendants of its own
- K020979: Sysmex Automated Coagulation Analyzer, Model #CA-7000 (2002), 1 descendant of its own

Source page: https://510kreport.com/device/K926551
Methodology: https://510kreport.com/methodology