Promex, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
9 devices
Cleared
Jul 24, 2001
VACUUM ASSISTED CORE BIOPSY DEVICE
Gastroenterology & Urology
162d
Cleared
Jun 22, 2001
AUTOMATED CORE BIOPSY DEVICE
Gastroenterology & Urology
57d
Cleared
May 01, 2000
BONE BIOPSY NEEDLE
Gastroenterology & Urology
21d
Cleared
Jan 07, 2000
AUTOMATED CORE BIOPSY DEVICE
Gastroenterology & Urology
18d
Cleared
Dec 06, 1999
MANUAL BONE MARROW BIOPSY DEVICE
Gastroenterology & Urology
55d
Cleared
Sep 29, 1995
TROCAR STYLE NEEDLE/CO-AXIAL INTRODUCER NEEDLE
Gastroenterology & Urology
17d
Cleared
Sep 22, 1995
AUGASTROENTEROLOGY-UROLOGY BIOPSY INSTRUMENT
Gastroenterology & Urology
11d
Cleared
Sep 12, 1995
GREENE, TURNER, MENGHINI STYLE ASPIRATION BIOPSY NEEDLE
Gastroenterology & Urology
7d
Cleared
Dec 21, 1994
CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLE
Gastroenterology & Urology
62d