510(k) K070800
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