Gallini U.S., LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gallini U.S., LLC - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Gallini U.S., LLC has 10 FDA 510(k) cleared gastroenterology & urology devices. Based in Glen Allen, US.
Historical record: 10 cleared submissions from 1997 to 1999.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gallini U.S., LLC
10 devices
Cleared
Aug 12, 1999
GALLINI BIOSYSTEM BONE MARROW ASPIRATION/BIOPSY NEEDLE
Gastroenterology & Urology
17d
Cleared
May 19, 1999
GALLINI ATRA-CUT NEEDLE
Gastroenterology & Urology
82d
Cleared
May 17, 1999
GALLINI BYCUT NEEDLE
Gastroenterology & Urology
74d
Cleared
Jul 08, 1998
SPEED-CUT AUTOMATIC BIOPSY SYSTEM
Gastroenterology & Urology
90d
Cleared
May 21, 1998
SPIGAL NEEDLE
Gastroenterology & Urology
90d
Cleared
May 06, 1998
QUICK-CUT AUTOMATIC BIOPSY SYSTEM
Gastroenterology & Urology
89d
Cleared
Feb 18, 1998
ACRI R NEEDLE
Gastroenterology & Urology
26d
Cleared
Jan 30, 1998
IBI
Gastroenterology & Urology
66d
Cleared
Jan 09, 1998
GALLINI ABS DEVICE
Gastroenterology & Urology
140d
Cleared
Jul 29, 1997
GALLINI COAXIAL INTRODUCER
Gastroenterology & Urology
42d