Derata Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Derata Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Derata Corp. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1988. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Derata Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Derata Corp.
6 devices
Cleared
Oct 31, 1988
DERATA MEDI-JECTOR V
General Hospital
49d
Cleared
Feb 19, 1987
DERATA MEDI-JECTOR IV
General Hospital
92d
Cleared
Jul 05, 1985
DERATA MEDI-JECTOR PRO
General Hospital
246d
Cleared
Nov 28, 1984
DERATA MEDI-JECTOR III
General Hospital
36d
Cleared
Mar 06, 1984
MEDI-JECTOR II
General Hospital
104d
Cleared
Dec 08, 1977
MEDI-JECTOR
General Hospital
27d