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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact