Dana Products, Inc. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dana Products, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Dana Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in South Barrington, US.
Historical record: 9 cleared submissions from 2002 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Dana Products, Inc. Filter by specialty or product code using the sidebar.
Dana Products, Inc. — FDA 510(k) Products and Clearance History
9 devices
Cleared
Feb 11, 2014
DANA REUSABLE TEST PACK
General Hospital
110d
Cleared
Nov 25, 2013
DANA REUSABLE BI TEST PACK
General Hospital
311d
Cleared
Feb 27, 2013
DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS
General Hospital
365d
Cleared
Apr 29, 2011
REUSABLE TEST PACK FOR DANA EMULATING INDICATORS
General Hospital
91d
Cleared
Feb 16, 2011
DANA REUSABLE TESTPACK FOR STEAM STERILIZATION FOR 10 MINUTE EXTENDED CYCLES
General Hospital
96d
Cleared
Jan 13, 2011
DANA EMULATING INDICATOR
General Hospital
288d
Cleared
Dec 20, 2010
DANA REUSABLE TEST PACK FOR STEAM STERILIZATION
General Hospital
88d
Cleared
Mar 18, 2010
DANA REUSABLE TEST PACK FOR STEAM STERILIZATION
General Hospital
175d
Cleared
May 07, 2002
STEAM STERILIZATION INTERGRATOR
General Hospital
298d