# K991895: Rampipella, Singe Port (720196) & Wedge-Shaped Port (720217)

- Pathway: 510(k) (Traditional)
- Applicant: Ri Mos. S.R.L.
- Decided: Aug 12, 1999 after 70 days
- Product code: HHK (Curette, Suction, Endometrial (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1175
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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 its predicate without a number.
- (no number) Unimar Pipelle® Pipelle de Cornier™ Endometrial Suction Curette: named in the summary without a submission number
- (no number) Vabra Aspirator®: named in the summary without a submission number

## Most influential descendants
- K992926: Ginram Endocic Single Oval Port (Model NO. 720195) (1999), 0 descendants of its own

## Indications for use
For endometrial sampling for histologic biopsy of the uterine mucosal lining.

Source page: https://510kreport.com/device/K991895
Methodology: https://510kreport.com/methodology