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Mediplus , Ltd.

FDA Regulatory Profile

Mediplus , Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 17, 2014.

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

FDA data resources