Amedic USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Amedic USA
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