510(k) K000040

INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED by Indus Medicare , Ltd. — Product Code HIS

K000040 is an FDA 510(k) premarket notification submitted by Indus Medicare , Ltd. for the device "INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED". The FDA issued a decision of Substantially Equivalent on March 21, 2000. The device falls under product code HIS (Condom), a Class II device regulated under 21 CFR 884.5300. Indus Medicare , Ltd. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 21, 2000
Date Received
January 6, 2000
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Condom
Device Class
Class II
Regulation Number
884.5300
Review Panel
OB
Submission Type