Indus Medicare , Ltd. is one of 94 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Indus Medicare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: INVIGRA, INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT), INVIGRA
8
Total
8
Cleared
0
Denied
Indus Medicare , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Hyderabad Andhra Pradesh, IN.
Historical record: 8 cleared submissions from 1999 to 2003. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Indus Medicare , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Indus Medicare , Ltd.
8 devices
Cleared
Apr 08, 2003
INVIGRA
Obstetrics & Gynecology
245d
Cleared
Mar 04, 2002
INVIGRA
Obstetrics & Gynecology
41d
Cleared
Mar 21, 2000
INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED
Obstetrics & Gynecology
75d
Cleared
Mar 21, 2000
INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED
Obstetrics & Gynecology
75d
Cleared
Mar 21, 2000
INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED
Obstetrics & Gynecology
75d
Cleared
Dec 29, 1999
INVIGRA
Obstetrics & Gynecology
57d
Cleared
Aug 02, 1999
INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)
Obstetrics & Gynecology
11d
Cleared
Jun 15, 1999
INVIGRA
Obstetrics & Gynecology
55d