# K980192: Manan Nephrostomy Drainage Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Medical Device Technologies, Inc.
- Decided: May 27, 1998 after 127 days
- Product code: LJE (Catheter, Nephrostomy)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K953547 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K953547: Manan Nephrostomy Drainage Catheter, Manan Medical Products, Inc. (1995) Summary page 1.

## Indications for use
The Manan™ Nephrostomy Drainage Catheter is for percutaneous nephrostomy.

Source page: https://510kreport.com/device/K980192
Methodology: https://510kreport.com/methodology