# K990411: MVM 7.5 French Flexible Hysteroscope

- Pathway: 510(k) (Traditional)
- Applicant: Karl Storz Endoscopy
- Decided: May 11, 1999 after 90 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.
24 later devices descend from it; 2 cite it directly.
0 of 25 devices 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.

## Most influential descendants
- K092278: Gyrus Acmi Invisio Digital Hysteroscope, Model Idh-4 (2009), 22 descendants of its own
- K123151: Endosee Model 8000 U-Scope (2013), 20 descendants of its own
- K132384: U-Scope 8000 System with HSC+Emb Cannula (2014), 19 descendants of its own
- K170660: Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula (2017), 5 descendants of its own
- K202445: Hystero-V Hysteroscope (2021), 4 descendants of its own

## Indications for use
This instrument is indicated for examination of the cervix and uterus and, using additional accessories, to perform various diagnostic and therapeutic procedures including; Diagnostic Hysteroscopy abnormal uterine bleeding infertility and pregnancy wastage evaluvation of abnormal hysterosalpingogram intrauterine foreign body amenorrhea pelvic pain evaluation of abnormalities of the endometrium monitoring IUD status Operative Hysteroscopy directed biopsy removal of submucous fibroids and large polps submucous myomectomy transection of intrauterine adhesions transection of intrauterine septa endometrial ablation

Source page: https://510kreport.com/device/K990411
Methodology: https://510kreport.com/methodology