510(k) K070800

LIFESTYLES LUBRICATED POLYISOPRENE LATEX MALE CONDOM by Ansell Healthcare Products, LLC — Product Code MOL

K070800 is an FDA 510(k) premarket notification submitted by Ansell Healthcare Products, LLC for the device "LIFESTYLES LUBRICATED POLYISOPRENE LATEX MALE CONDOM". The FDA issued a decision of Substantially Equivalent on March 6, 2008. The device falls under product code MOL (Condom, Synthetic), a Class II device regulated under 21 CFR 884.5300. Ansell Healthcare Products, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 6, 2008
Date Received
March 23, 2007
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

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