Advanced Clinical Diagnostics is one of 13502 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Clinical Diagnostics - FDA 510(k) Cleared Devices
Recent clearances: RHESUS MONKEY KIDNEY CELLS, TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY, RHESUS MONKEY KIDNEY CELLS (LLC-MK2)
19
Total
19
Cleared
0
Denied
Advanced Clinical Diagnostics has 19 FDA 510(k) cleared pathology devices. Based in Toledo, US.
Historical record: 19 cleared submissions from 1988 to 1994.
Browse the complete list of FDA 510(k) cleared pathology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advanced Clinical Diagnostics
19 devices
Cleared
Feb 03, 1994
RHESUS MONKEY KIDNEY CELLS
Pathology
42d
Cleared
Feb 03, 1994
TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY
Pathology
42d
Cleared
Feb 03, 1994
RHESUS MONKEY KIDNEY CELLS (LLC-MK2)
Pathology
42d
Cleared
Jan 28, 1994
RABBIT KIDNEY CELLS - R.K.C.
Pathology
155d
Cleared
Jan 28, 1994
HELA-229/HELA CELLS
Pathology
102d
Cleared
Jan 24, 1994
PRIMARY AFRICAN GREEN MONKEY KIDNEY CELLS
Pathology
80d
Cleared
Jan 03, 1994
KIDNEY AFRICAN GREEN MONKEY CELLS-CV-1
Pathology
130d
Cleared
Jan 03, 1994
KIDNEY AFRICIAN GREEN MONKEY CELLS-VERO
Pathology
130d
Cleared
Jan 03, 1994
MCCOY CULTURE CELLS-MCCOY
Pathology
130d
Cleared
Jan 03, 1994
BUFFALO GREEN MONKEY KIDNEY CELLS-B.G.M.K.
Pathology
130d
Cleared
Jan 03, 1994
HUMAN EPIDERMAL CARCINOMA LARYNX CELLS-HEP-2
Pathology
130d
Cleared
Jan 03, 1994
HUMAN LUNG DIPLOID CELLS-MRC-5
Pathology
130d