Devon Medical, Inc. is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Devon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: extriCARE 2400 NPWT System with extriCARE 2400 NPWT Pump and extriCARE NPWT Foam Dressing Kit, EXTRICARE, EXTRICARE NPWT FOOT DRESSING
11
Total
11
Cleared
0
Denied
Devon Medical, Inc. has 11 FDA 510(k) cleared cardiovascular devices. Based in King Of Prussia, US.
Historical record: 11 cleared submissions from 2009 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Devon Medical, Inc.
11 devices
Cleared
Sep 19, 2014
extriCARE 2400 NPWT System with extriCARE 2400 NPWT Pump and extriCARE NPWT...
General & Plastic Surgery
191d
Cleared
May 15, 2014
EXTRICARE
General & Plastic Surgery
302d
Cleared
Aug 13, 2013
EXTRICARE NPWT FOOT DRESSING
General & Plastic Surgery
84d
Cleared
Jul 01, 2013
CIRONA DVT FOOT GARMENT
Cardiovascular
18d
Cleared
Apr 09, 2013
DEVON CIRONA 6100 DVT
Cardiovascular
36d
Cleared
Feb 28, 2013
CIRCUFLOW 5150
Cardiovascular
69d
Cleared
Feb 14, 2013
CIRCUFLOW 5208 SEQUENTIAL COMPRESSION DEVICE
Cardiovascular
79d
Cleared
Oct 07, 2010
ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE
Cardiovascular
29d
Cleared
Jun 17, 2010
CIRCUFLOW 5200 SEQUENTIAL COMPRESSION DEVICE
Cardiovascular
15d
Cleared
Mar 05, 2010
CIRCUFLOW 5100 SEQUENTIAL COMPRESSION DEVICE
Cardiovascular
16d
Cleared
Mar 23, 2009
DEVON ACCUBP CUFF
Cardiovascular
10d