# K935070: Grasping Forceps, Biopsy Forceps, Spoon Forceps

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Jan 25, 1994 after 92 days
- Product code: FCL (Forceps, Biopsy, Non-Electric)
- Device class: 1
- 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.
12 later devices descend from it; 1 cites it directly.
0 of 13 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
- K973648: Mini Forceps with HF, 3.5MM; Micro Forceps with HF, 2MM (1997), 11 descendants of its own
- K980758: 3 MM Selec-Tip Laparoscopic Scissors (1998), 10 descendants of its own
- K014207: Reposable Instrument System, Models MF001-MF083 (2002), 8 descendants of its own
- K063485: Logic Laparoscopic Scissors (2006), 7 descendants of its own
- K090583: Endoscopic Monopolar Scissors, Models Ems-235, Ems-165 (2009), 4 descendants of its own

Source page: https://510kreport.com/device/K935070
Methodology: https://510kreport.com/methodology