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Promedic, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K131889EUM 100PROApril 23, 2014
K112318CLEARPATH 24June 29, 2012
K072756NON-IV ADAPTER FOR INFANT NG TUBEDecember 19, 2007
K060497BABYAIRJuly 11, 2006
K060842REVJET TURBOJune 21, 2006
K052903PEDIATRIC FEEDING TUBENovember 9, 2005
K031409URINARY CATHETERSJune 17, 2003
K024190FENESTRATED INFUSION CATHETERMarch 17, 2003
K023579GAS SAMPLING LINESJanuary 28, 2003
K020005INFANT FEEDING TUBESJuly 16, 2002
K970102FILTERJune 24, 1997
K970991DATEX ENGSTOM MANUAL RESUSCITATORJune 16, 1997
K962182BURLEW INFANT HOODJuly 15, 1996
K954201BUONAFEDE PNEUMATIC SLEEVENovember 9, 1995
K951988PRESSURIZERJune 14, 1995
K951043AIR-SOFT-DISPOSABLE, ANESTHESISA/RESPIRATORY FACE MASKJune 7, 1995