Applied Medical Devices, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Applied Medical Devices, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1979 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Applied Medical Devices, Inc. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Dec 19, 1984
PERCUTANEOUS ASPIRATION BIOPSY TRAY
General & Plastic Surgery
78d
Cleared
Dec 13, 1984
STERILE PERCUTANEOUS TRANSHEPATIC CHOLAN
General & Plastic Surgery
72d
Cleared
Dec 13, 1984
GENERAL UTILITY TRAY SYSTEM
General & Plastic Surgery
72d
Cleared
Aug 16, 1984
ACCU-CULT FECAL OCCULT BLOOD TEST
Hematology
170d
Cleared
Jul 23, 1984
ULTRASOUND PROBE COVERS-STERILE
Radiology
20d
Cleared
May 30, 1984
TRANSTHORACIC/TRANSABDOMINAL-TRAY
General & Plastic Surgery
219d
Cleared
Apr 13, 1984
CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY
General Hospital
79d
Cleared
Feb 09, 1984
PREPACELL-STERILE-BONE MARROW ASPIR
General & Plastic Surgery
127d
Cleared
Jan 25, 1984
PREPACELL THIN NEEDLE ASPIRATION TRAY
Gastroenterology & Urology
93d
Cleared
Jan 15, 1981
CYTOTRAN I BONE MARROW ASPIRATION SYSTEM
General Hospital
104d
Cleared
Sep 12, 1979
PREPACELL-BONE MARROW SAMPLER
General Hospital
22d