# K913101: Peters Cardioflon (TM) Suture

- Pathway: 510(k) (Traditional)
- Applicant: Promedica Products, Inc.
- Decided: Aug 12, 1992 after 397 days
- Product code: GAS (Suture, Nonabsorbable, Synthetic, Polyester)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K060163: Cardioflon, Cardioxyl (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K913101
Methodology: https://510kreport.com/methodology