Medical Device Manufacturer · IN , Hyderabad Andhra Pradesh

Indus Medicare , Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1999
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
1-8 of 8
Cleared Apr 08, 2003
INVIGRA
K022614 · HIS
Obstetrics & Gynecology · 245d
Cleared Mar 04, 2002
INVIGRA
K020223 · HIS
Obstetrics & Gynecology · 41d
Cleared Mar 21, 2000
INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED
K000038 · HIS
Obstetrics & Gynecology · 75d
Cleared Mar 21, 2000
INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED
K000039 · HIS
Obstetrics & Gynecology · 75d
Cleared Mar 21, 2000
INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED
K000040 · HIS
Obstetrics & Gynecology · 75d
Cleared Dec 29, 1999
INVIGRA
K993693 · HIS
Obstetrics & Gynecology · 57d
Cleared Aug 02, 1999
INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)
K992438 · LTZ
Obstetrics & Gynecology · 11d
Cleared Jun 15, 1999
INVIGRA
K991374 · HIS
Obstetrics & Gynecology · 55d
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