# K792159: Fisch Drill System

- Pathway: 510(k) (Traditional)
- Applicant: Jedmed Instrument Co.
- Decided: Nov 27, 1979 after 29 days
- Product code: ERL (Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece)
- Device class: 2
- Regulation: 21 CFR 874.4250
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K984244: Orl-E-92 Surgical Drill System (1999), 1 descendant of its own
- K031540: Apex Electric Handpiece System (2003), 0 descendants of its own

## Recalls of this device
- Sep 11, 2020 · Class II · Z-0176-2021: The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

Source page: https://510kreport.com/device/K792159
Methodology: https://510kreport.com/methodology