Mckinley, Inc. is one of 21549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mckinley, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BEELINE MOTIV, PROPOLIS, PCA, MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS, BEELINE SYSTEM
7
Total
7
Cleared
0
Denied
Mckinley, Inc. has 7 FDA 510(k) cleared medical devices. Based in Wheat Ridge, US.
Historical record: 7 cleared submissions from 1998 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Mckinley, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mckinley, Inc.
7 devices
Cleared
Nov 08, 2004
BEELINE MOTIV, PROPOLIS, PCA
General Hospital
83d
Cleared
Oct 07, 2003
MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS
General Hospital
8d
Cleared
Sep 23, 2003
BEELINE SYSTEM
General Hospital
27d
Cleared
Jul 01, 1999
WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS
General Hospital
78d
Cleared
Jun 30, 1999
MCKINLEY SP DISPOSABLE INFUSION PUMP
General Hospital
138d
Cleared
Sep 30, 1998
OUTBOUND DISPOSABLE SYRINGE INFUSER OUTBOUND 2 DISPOSABLE PUMP
General Hospital
96d
Cleared
Jan 23, 1998
MCKINLEY OUTBOUND-2 SYSTEM
General Hospital
249d