# K953370: Karl Storz Ent Shaver

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Sep 6, 1995 after 50 days
- Product code: EQJ (Bur, Ear, Nose And Throat)
- Device class: 1
- Regulation: 21 CFR 874.4140
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 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
- K984521: Riwo Drive System 2302 with Generator, Small Motor Handles, 8563.111, 8563.351 (1999), 9 descendants of its own
- K030082: Power Control 2303 with Power Stick M4, Model# 2303.011/.901/.911, 8564.121/.851 (2003), 8 descendants of its own
- K041610: Morce Scope Set 8970 with Power Control 2303 and Suction Pump 2207 (2004), 6 descendants of its own
- K192499: Cyber Blade (2020), 2 descendants of its own
- K213597: MultiCut Solo (2023), 1 descendant of its own

Source page: https://510kreport.com/device/K953370
Methodology: https://510kreport.com/methodology