# K000163: PM 2002 Proline/Aec

- Pathway: 510(k) (Traditional)
- Applicant: Planmeca Oy
- Decided: Apr 18, 2000 after 90 days
- Product code: EHD (Unit, X-Ray, Extraoral With Timer)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K051464: Planmeca Promax with Dec (Dynamic Exposure Control) (2005), 1 descendant of its own
- K072244: Planmeca Proone (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K000163
Methodology: https://510kreport.com/methodology