FDA 510(k) Applications Submitted by MCKINLEY, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K033039 |
09/29/2003 |
MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS |
MCKINLEY, INC. |
K032642 |
08/27/2003 |
BEELINE SYSTEM |
MCKINLEY, INC. |
K971844 |
05/19/1997 |
MCKINLEY OUTBOUND-2 SYSTEM |
MCKINLEY, INC. |
K990461 |
02/12/1999 |
MCKINLEY SP DISPOSABLE INFUSION PUMP |
MCKINLEY, INC. |
K991275 |
04/14/1999 |
WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS |
MCKINLEY, INC. |
K042228 |
08/17/2004 |
BEELINE MOTIV, PROPOLIS, PCA |
MCKINLEY, INC. |
K982256 |
06/26/1998 |
OUTBOUND DISPOSABLE SYRINGE INFUSER OUTBOUND 2 DISPOSABLE PUMP |
MCKINLEY, INC. |
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