Skip to content

Company · IN

Indus Medicare , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2003. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
HIS	Condom	7
LTZ	Condom With Nonoxynol-9	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Apr 8, 2003	K022614	INVIGRA Indus Medicare , Ltd., IN	HIS
Mar 4, 2002	K020223	INVIGRA Indus Medicare , Ltd., IN	HIS
Mar 21, 2000	K000040	INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED Indus Medicare , Ltd., IN	HIS
Mar 21, 2000	K000039	INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED Indus Medicare , Ltd., IN	HIS
Mar 21, 2000	K000038	INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED Indus Medicare , Ltd., IN	HIS
Dec 29, 1999	K993693	INVIGRA Indus Medicare , Ltd., IN	HIS
Aug 2, 1999	K992438	INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT) Indus Medicare , Ltd., IN	LTZ
Jun 15, 1999	K991374	INVIGRA Indus Medicare , Ltd., IN	HIS

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

Get alerts for these product codes