# K952186: HSW GMBH Hysteroscopes & Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Henke-Sass, Wolf GmbH
- Decided: Feb 6, 1996 after 273 days
- Product code: HIH (Hysteroscope (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K091465: Myosure Rod Lens Hysteroscope (2009), 4 descendants of its own
- K122563: Myosure XL Rod Lens Hysteroscope, Myosure XL Outlfow Channel (2012), 2 descendants of its own
- K182006: Omni Hysteroscope, Omni Hysteroscope Kits, Omni Sheaths (2018), 1 descendant of its own
- K191281: Omni Hysteroscope, Omni Lok cervical seal (2019), 0 descendants of its own
- K102686: Myosure Rod Lens Scope Seals (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K952186
Methodology: https://510kreport.com/methodology