# P820009: Lincoff-Design Scleral Buckling Balloon Catheter

- Pathway: PMA
- Applicant: Bausch & Lomb
- Decided: Oct 25, 1983 after 610 days
- Product code: LOG (Catheter, Balloon For Retinal Reattachment)
- Device class: 3
- 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. PMA decisions do not claim a predicate device.

## Most influential descendants
- K990202: Sugita Titanium Aneurysm Clip (1999), 0 descendants of its own

Source page: https://510kreport.com/device/P820009
Methodology: https://510kreport.com/methodology