# K832187: Hall Oscillator

- Pathway: 510(k) (Traditional)
- Applicant: Amsco Co.
- Decided: Aug 12, 1983 after 37 days
- Product code: GET (Motor, Surgical Instrument, Pneumatic Powered)
- Device class: 1
- Regulation: 21 CFR 878.4820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K032607: Powerpro Pneumatic System, Models PRO6150, PRO6175, PRO6185 (2003), 6 descendants of its own
- K062842: Twist Drill (2006), 5 descendants of its own
- K213072: 2.1 x 255mm Drill, 22mm Stop (2022), 1 descendant of its own
- K223199: 2.1 x 255mm Drill, 22mm Stop (2022), 0 descendants of its own
- K213208: Twist Drills (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K832187
Methodology: https://510kreport.com/methodology