Amedic USA - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Amedic USA has 10 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Historical record: 10 cleared submissions from 1987 to 1990. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Amedic USA Filter by specialty or product code using the sidebar.
10 devices
Cleared
Jan 04, 1990
EQUIP COVERS, STERILE
General Hospital
9d
Cleared
Sep 05, 1989
GENERAL IVT NEEDLE GUIDE KIT, STERILE
Obstetrics & Gynecology
158d
Cleared
Aug 08, 1989
EXTENDED COVERS, STERILE
Gastroenterology & Urology
130d
Cleared
Aug 08, 1989
GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILE
Gastroenterology & Urology
130d
Cleared
Aug 04, 1989
TRT (ACUSON) NEEDLE GUIDE KIT, STERILE
Gastroenterology & Urology
127d
Cleared
Aug 21, 1987
BIOPSY NEEDLE GUIDE KIT, STERILE
Gastroenterology & Urology
129d
Cleared
Jul 15, 1987
ULTRASOUND TRANSDUCER GEL, STERILE
General & Plastic Surgery
84d
Cleared
Jul 15, 1987
ULTRASOUND TRANSDUCER SHEATHS, STERILE
Radiology
82d
Cleared
Jul 10, 1987
BIOPSY NEEDLE GUIDE KIT, STERILE
General & Plastic Surgery
84d
Cleared
Mar 27, 1987
TRANSVAGINAL ULTRASOUND BIOPSY NEEDLE GUIDE
Obstetrics & Gynecology
150d