# K882061: Olympus GF-UM3/EU-M3

- Pathway: 510(k) (Traditional)
- Applicant: Olympus Corp.
- Decided: Nov 15, 1988 after 183 days
- Product code: GDB (Endoscope, Fiber Optic)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
149 later devices descend from it; 3 cite it directly.
6 of 150 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
- K982323: Olympus UM 2R/3R Ultrasonic Probes and Associated Ancillary Equipment, for Bronchial Use (1998), 142 descendants of its own
- K042438: Superdimension/Bronchus (2004), 73 descendants of its own
- K982610: Olympus UM-2R/3R Ultrasonic Probes and Associated Ancillary Equipment (Urinary Tract) (1998), 67 descendants of its own
- K011886: Olympus EU-M60 Eus Exera Endoscopic Ultrasound CTR, Eus Exera Ultrasonic Gastrovideoscope Olympus GF Type UM 160, (2001), 60 descendants of its own
- K010591: Olympus EU-C60 Eus Exera Compact Endoscopic Ultrasound Center (2001), 59 descendants of its own

Source page: https://510kreport.com/device/K882061
Methodology: https://510kreport.com/methodology