Suretex Prophylactics (India) , Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Suretex Prophylactics (India) , Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Suretex Prophylactics (India) , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Bangalore, Karnataka, IN.
Historical record: 3 cleared submissions from 1998 to 1999. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Suretex Prophylactics (India) , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Suretex Prophylactics (India) , Ltd.
3 devices
Cleared
Aug 19, 1999
VARIOUS ANSELL TRADENAMES OR PRIVATE LABEL
Obstetrics & Gynecology
59d
Cleared
Dec 11, 1998
ROYALE BRAND LATEX CONDOMS SILICONE LUBRICANT COLORED-OR ASSORTED COLORS
Obstetrics & Gynecology
81d
Cleared
Jun 19, 1998
ROYALE OF LATEX CONDOMS - SPERMICIDAL LUBRICANT - COLORED OR ASSORTED COLORS
Obstetrics & Gynecology
44d