Microvena Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microvena Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Microvena Corp. has 18 FDA 510(k) cleared cardiovascular devices. Based in Findley, US.
Historical record: 18 cleared submissions from 1990 to 1999.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microvena Corp.
18 devices
Cleared
Jun 16, 1999
ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE
Cardiovascular
12d
Cleared
May 05, 1999
MODIFICATION TO ULTRA-SELECT GUIDEWIRE
Cardiovascular
27d
Cleared
Nov 18, 1998
AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT...
Cardiovascular
111d
Cleared
Jun 10, 1998
THE AMPLANTZ GOOSE NECK MICROSNARE
Cardiovascular
471d
Cleared
Mar 06, 1998
AMPLATZ GOOSE NECK SNARE KIT/ CATHETER
Cardiovascular
246d
Cleared
Sep 19, 1997
AMPLATZ THROMBECTOMY DEVICE(ATD 603,602,801,802)/FOOT PEDAL ASSEMBLY(AK 200)
Cardiovascular
113d
Cleared
Dec 17, 1996
HYDRO-SELECT GUIDEWIRE
Cardiovascular
434d
Cleared
Aug 13, 1996
THE AMPLATZ THROMBECTOMY DEVICE
Cardiovascular
341d
Cleared
May 16, 1996
CRICKET
Cardiovascular
178d
Cleared
Dec 13, 1995
THE NINER NITINOL GUIDEWIRE
Cardiovascular
174d
Cleared
Mar 31, 1995
M-PATH NITINOL GUIDEWIRE
Cardiovascular
91d
Cleared
Sep 24, 1993
MICROSNARE
Cardiovascular
331d
Cleared
Feb 23, 1993
.25' ULTRA-SELECT GUIDEWIRE
Cardiovascular
295d
Cleared
Nov 08, 1991
THE BIG EASY Y-ADAPTER
Cardiovascular
59d
Cleared
Apr 19, 1991
ULTRA-SELECT PTCA GUIDEWIRE
Cardiovascular
86d
Cleared
Dec 03, 1990
AMPLATZ GOOSE-NECK SNARE
Cardiovascular
249d
Cleared
May 09, 1990
UNIVERSAL DELIVERY SYSTEM CATHETER
Cardiovascular
89d
Cleared
Apr 10, 1990
SOLOSTICK (AMPLATZ DILATOR NEEDLE)
Cardiovascular
172d