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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 Jan 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 SETJan 17, 2014
K131339CAPNOMASKNov 25, 2013
K031617MEDIPLUS SINGLE USE LOWER GI MANOMETRY CATHETERJan 16, 2004
K013704MEDIPLUS SINGLE USE GI MANOMETRY CATHETERAug 5, 2002

FDA data resources