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Abbott Mfg., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K981457ALBPMay 27, 1998
K981232CAMay 18, 1998
K981231CO2May 12, 1998
K965230ABBOTT LIFECARE STANDARD TUBING INFUSION PUMPJuly 3, 1997
K971293LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVEJune 27, 1997
K953656ABBOTT IMX PROLACTIN(MODIFICATION)October 3, 1995
K953657ABBOTT AXSYM PROLACTIN(MODIFICATION)September 25, 1995
K944669FLEXIFLO QUANTUM ENTERAL PUMPJuly 24, 1995
K943691IMX FOLATEMarch 23, 1995
K943733FLEXIFLO SIX ENTERAL NUTRITION PUMPDecember 12, 1994
K941214LIFESHIELD EXTENSION SETOctober 3, 1994
K940289ABBOTT PRISM ANALYZERJuly 18, 1994
K935376AXSYM GENTAMICINJune 21, 1994
K902753IMX ULTRASENTITIVE HTSHJuly 10, 1990