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Mediplus , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K132890SUPRAPUBIC CATHETER AND INTRODUCER SETJanuary 17, 2014
K131339CAPNOMASKNovember 25, 2013
K031617MEDIPLUS SINGLE USE LOWER GI MANOMETRY CATHETERJanuary 16, 2004
K013704MEDIPLUS SINGLE USE GI MANOMETRY CATHETERAugust 5, 2002