Turpen Laboratory Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Turpen Laboratory Systems, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Turpen Laboratory Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1987. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Turpen Laboratory Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Turpen Laboratory Systems, Inc.
6 devices
Cleared
Apr 01, 1987
ATAC 1500 CHEMISTRY ANALYZER
Chemistry
29d
Cleared
Sep 29, 1986
ATAC 4300 HEMATOLOGY CELL COUNTER
Hematology
33d
Cleared
Apr 25, 1985
ATAC 2000 CHEMISTRY ANALYZER
Chemistry
23d
Cleared
Oct 11, 1984
ATAC 2000
Chemistry
69d
Cleared
Jan 10, 1984
ATAC 3000
Chemistry
194d
Cleared
Oct 20, 1983
ATAC 4700 HEMATOLOGY CELL COUNTER
Hematology
112d