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/ Medxl, Inc.
Medxl, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K233623
Praxiject SP 0.9% NaCl
February 27, 2024
K231754
Praxiject 0.9% NaCl
July 13, 2023
K192414
Praxiject 0.9% NaCl
February 13, 2020
K171109
Praxiject 0.9% NaCl
December 21, 2017