# K974312: Reusable Biopsy Forceps Oval Cup, Reusable Biosy Forceps Oval Cup W/Needle, Reusable Biopsy Forceps Serrated Cup, Reusar

- Pathway: 510(k) (Traditional)
- Applicant: Telemed Systems, Inc.
- Decided: Jan 21, 1998 after 65 days
- Product code: KNW (Instrument, Biopsy)
- Device class: 2
- Regulation: 21 CFR 876.1075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The TeleMed Systems, Inc. Reusable Biopsy Forceps are indicated for use in obtaining endoscopically tissue samples, retrieval of foreign bodies and stones from the GI and Urinary tracts and the lungs

Source page: https://510kreport.com/device/K974312
Methodology: https://510kreport.com/methodology