# K872712: PC Polygraf

- Pathway: 510(k) (Traditional)
- Applicant: Synectics-Dantec
- Decided: Mar 18, 1988 after 252 days
- Product code: KLA (Monitor, Esophageal Motility, Anorectal Motility, And Tube)
- Device class: 2
- Regulation: 21 CFR 876.1725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K972439: Anorectal Manometry Analysis Module (1997), 1 descendant of its own
- K992713: Polygraf ID, Polygram '98 Esophageal Manometry Testing Application, Models 9043G0121-9043G0151, 9043S0101 (1999), 0 descendants of its own
- K991389: Anorectal Manometry Suite, Model 9032S0201 (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K872712
Methodology: https://510kreport.com/methodology