# K952149: Karl Storz Take-Apart Rotating Grasping Forceps

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Jun 15, 1995 after 38 days
- Product code: LQR (Dislodger, Stone, Biliary)
- Device class: 2
- Regulation: 21 CFR 876.5010
- Recalls of this device: none
- 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
- K965176: Pilling Weck 2 Piece Take-Apart Instruments (1997), 1 descendant of its own
- K030919: Siss, Inc. (D.B.a.Medisiss) Reprocessd Electrosurgical Instruments and Accessories (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K952149
Methodology: https://510kreport.com/methodology