# K895415: Biopsy Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Symbiosis Corp.
- Decided: Oct 31, 1989 after 56 days
- Product code: EOQ (Bronchoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K102336: Radial Jaw 4 Pulmonary Standard Capacity Biopsy Forceps; Radial Jaw 4 Pulmonary Standard Capacity Biopsy Forceps with NE (2011), 2 descendants of its own
- K121186: Radial Jaw 4 Pulmonary Biopsy Forceps (2012), 1 descendant of its own
- K252921: Radial Jaw 4 Pulmonary Biopsy Forceps (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K895415
Methodology: https://510kreport.com/methodology