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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