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FDA 510(k) Applications Submitted by ABBOTT MFG., INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K965230
12/31/1996
ABBOTT LIFECARE STANDARD TUBING INFUSION PUMP
ABBOTT MFG., INC.
K981231
04/03/1998
CO2
ABBOTT MFG., INC.
K981232
04/03/1998
CA
ABBOTT MFG., INC.
K981457
04/23/1998
ALBP
ABBOTT MFG., INC.
K971293
04/07/1997
LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE
ABBOTT MFG., INC.
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