Promedic, Inc.

FDA Regulatory Profile

Promedic, Inc. appears in FDA public data with 0 recalls, 16 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 23, 2014.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K131889EUM 100PROApr 23, 2014
K112318CLEARPATH 24Jun 29, 2012
K072756NON-IV ADAPTER FOR INFANT NG TUBEDec 19, 2007
K060497BABYAIRJul 11, 2006
K060842REVJET TURBOJun 21, 2006
K052903PEDIATRIC FEEDING TUBENov 9, 2005
K031409URINARY CATHETERSJun 17, 2003
K024190FENESTRATED INFUSION CATHETERMar 17, 2003
K023579GAS SAMPLING LINESJan 28, 2003
K020005INFANT FEEDING TUBESJul 16, 2002
K970102FILTERJun 24, 1997
K970991DATEX ENGSTOM MANUAL RESUSCITATORJun 16, 1997
K962182BURLEW INFANT HOODJul 15, 1996
K954201BUONAFEDE PNEUMATIC SLEEVENov 9, 1995
K951988PRESSURIZERJun 14, 1995
K951043AIR-SOFT-DISPOSABLE, ANESTHESISA/RESPIRATORY FACE MASKJun 7, 1995