# K950335: Karl Storz Rigid Telescopes for Obsterics and Gynecology

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: May 16, 1996 after 475 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- 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. The FDA summary names no predicate by number.

## Indications for use
The Karl Storz Rigid Telescopes for Obstetrics and Gynecology and their predicate devices are designed to allow viewing of the site during laparoscopic and hysteroscopic surgical procedures.

Source page: https://510kreport.com/device/K950335
Methodology: https://510kreport.com/methodology