Drg Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Drg Intl., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Drg Intl., Inc. has 4 FDA 510(k) cleared medical devices. Based in East Stroudsburg, US.
Historical record: 4 cleared submissions from 2000 to 2008. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Drg Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Drg Intl., Inc.
4 devices
Cleared
Jan 29, 2008
ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY 17-A-HYDROXYPROGESTERONE
Chemistry
518d
Cleared
Jan 27, 2006
DRG SLV TESTOSTERONE ELISA TEST
Chemistry
123d
Cleared
Dec 07, 2005
ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY CORTISOL
Chemistry
162d
Cleared
Apr 17, 2000
DRG AURICA ELISA TESTOSTERONE KIT
Chemistry
102d