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