Copan Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Copan Diagnostics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Copan Diagnostics, Inc. has 10 FDA 510(k) cleared microbiology devices. Based in North Attleboro, US.
Historical record: 10 cleared submissions from 1995 to 2006.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Copan Diagnostics, Inc.
10 devices
Cleared
Jun 23, 2006
COPAN LIQUID AMIES ELUTION SWAB (ESWAB) COLLECTION AND TRANSPORT SYSTEM
Microbiology
44d
Cleared
Dec 07, 2004
COPAN UNIVERSAL TRANSPORT MEDIUM (UTM-RT) SYSTEM
Microbiology
40d
Cleared
Jul 31, 2001
COPAN VIRAL TRANSYSTEM
Microbiology
413d
Cleared
Nov 09, 1999
COPAN EASY-SWAB COLLECTION AND TRANSPORT SYSTEM
Microbiology
48d
Cleared
Mar 10, 1995
COPAN VENTURI TRANSYSTEM LIQUID STUARTS MEDIUM
Microbiology
73d
Cleared
Mar 10, 1995
COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL
Microbiology
73d
Cleared
Mar 10, 1995
COPAN VENTURI TRANSYSTEM STUARTS MEDIUM
Microbiology
73d
Cleared
Mar 10, 1995
COPAN VENTURI TRANSYSTEM CARY-BLAIR MEDIUM
Microbiology
73d
Cleared
Mar 10, 1995
COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITHOUT CHARCOAL
Microbiology
73d
Cleared
Mar 10, 1995
COPAN VENTURI TRANSYSTEM LIQUID AMIES MEDIUM
Microbiology
73d