Vascular Technology Incorporated is one of 22251 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vascular Technology Incorporated - FDA 510(k) Cleared Devices
Recent clearances: VTI INTRAOPERATIVE DOPPLER SYSTEMS, VTI 20 MHZ GATED DOPPLER, VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000
11
Total
11
Cleared
0
Denied
Vascular Technology Incorporated has 11 FDA 510(k) cleared medical devices. Based in Attleboro, US.
Historical record: 11 cleared submissions from 1985 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vascular Technology Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vascular Technology Incorporated
11 devices
Cleared
Oct 28, 2008
VTI INTRAOPERATIVE DOPPLER SYSTEMS
Cardiovascular
29d
Cleared
Apr 23, 2003
VTI 20 MHZ GATED DOPPLER
Cardiovascular
16d
Cleared
Nov 06, 2000
VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000
Neurology
42d
Cleared
Dec 27, 1994
VTI DISPOSABLE PRESSURE DISPLAY SET
Cardiovascular
91d
Cleared
Jan 27, 1993
VTI OXYGEN ANALYZER
Anesthesiology
233d
Cleared
Nov 21, 1989
VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM
Anesthesiology
319d
Cleared
Oct 04, 1989
GIPHY MONITOR
Gastroenterology & Urology
379d
Cleared
May 11, 1987
CARDIAC PERFORMANCE MONITOR
Cardiovascular
172d
Cleared
Jun 25, 1986
KHURI REGIONAL TISSUE PH MONITOR
Anesthesiology
22d
Cleared
Jun 19, 1986
NO. 100352 GALVANIC OXYGEN SENSOR
Anesthesiology
16d
Cleared
Jun 20, 1985
VASCULAR TECH # 100123 POLAROGRAPHIC OXGYEN SENSOR
Anesthesiology
22d