# K962587: Conceptus Fallopian Tube Catheteization with Microendoscopy System

- Pathway: 510(k) (Traditional)
- Applicant: Conceptus, Inc.
- Decided: Jan 31, 1997 after 214 days
- Product code: MKO (Falloposcope)
- 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.
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) Conceptus FTC System: named in the summary without a submission number

## Most influential descendants
- K221965: FemDx FalloView (2023), 0 descendants of its own

## Indications for use
The Conceptus FTCM System is intended for use in selective catheterization/cannulation of the fallopian tubes in order to evaluate proximal tubal occlusion or patency under direct visualization.

Source page: https://510kreport.com/device/K962587
Methodology: https://510kreport.com/methodology