# K882517: Rodenstock Scanning Laser Ophthalmoscope

- Pathway: 510(k) (Traditional)
- Applicant: Rodenstock Instrument Corp.
- Decided: Jan 24, 1989 after 221 days
- Product code: HLI (Ophthalmoscope, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 3 cite it directly.
0 of 16 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
- K983999: PANORAMIC200 Opthalmoscope (1999), 13 descendants of its own
- K100644: Optos Limited Panoramic 200CAF (2010), 9 descendants of its own
- K042001: Panoramic 200A (2004), 9 descendants of its own
- K060424: Panoramic, Model 200MA (2006), 8 descendants of its own
- K102492: P200MAAF (2010), 7 descendants of its own

Source page: https://510kreport.com/device/K882517
Methodology: https://510kreport.com/methodology