Medical Device Technologies, Inc. - FDA 510(k) Cleared Devices
46
Total
46
Cleared
0
Denied
Medical Device Technologies, Inc. has 46 FDA 510(k) cleared medical devices. Based in Gainsville, US.
Historical record: 46 cleared submissions from 1992 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medical Device Technologies, Inc. Filter by specialty or product code using the sidebar.
46 devices
Cleared
Aug 27, 2010
BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT
Gastroenterology & Urology
57d
Cleared
Jan 26, 2006
INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
General & Plastic Surgery
38d
Cleared
Aug 30, 2005
INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
General & Plastic Surgery
90d
Cleared
May 26, 2005
CANALIZER HYDROPHILIC GUIDE WIRE
Cardiovascular
50d
Cleared
Feb 11, 2005
INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE
Gastroenterology & Urology
53d
Cleared
Sep 30, 2004
V-CORE FULL CORE BREAST BIOPSY INSTRUMENT
Gastroenterology & Urology
17d
Cleared
May 03, 2004
FIBREX CATHETER PATENCY DEVICE
General Hospital
74d
Cleared
Aug 13, 2003
PBN GUIDEWIRES
Cardiovascular
99d
Cleared
May 31, 2002
EN-SNARE ENDOVASCULAR SNARE AND CATHETER
Cardiovascular
15d
Cleared
Sep 05, 2001
MICROCRUISER PLUS INTRODUCER SET
Cardiovascular
89d
Cleared
Oct 30, 2000
PBN FALLOPIAN TUBE CATHETER SYSTEM
Obstetrics & Gynecology
249d
Cleared
Sep 11, 2000
GOLDEN-RULE SCALING CATHETER
Cardiovascular
34d
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