# K992904: Mini-Port

- Pathway: 510(k) (Traditional)
- Applicant: Taut, Inc.
- Decided: Oct 5, 1999 after 36 days
- Product code: GBW (Catheter, Peritoneal)
- Device class: 1
- Regulation: 21 CFR 878.4200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K070686: Mini Lap Instruments (2007), 6 descendants of its own
- K113597: Mini-Lap Bipolar Electrocautery Devices (2012), 1 descendant of its own
- K070352: Mini Lap Pediatric Instruments with Medusa Clamping System (2007), 1 descendant of its own
- K172775: MiniLap System with MiniGrip Handle, MiniLap System with ThumbGrip Handle (2018), 0 descendants of its own
- K160149: Miret Grasper, Alligator, Miret Grasper, Maryland (2016), 0 descendants of its own

## Indications for use
For use as an abdominal access port during a laparoscopic procedure and the 1-way stopcock for attaching insufflation tubing to maintain pneumoperitoneal pressure.

Source page: https://510kreport.com/device/K992904
Methodology: https://510kreport.com/methodology