510(k) K030176
K030176 is an FDA 510(k) premarket notification submitted by Suretex, Ltd. for the device "LIFESTYLES, CONTEMPO OR PRIVATE LABEL-MALE LATEX CONDOM WITH DESENSITIZING LUBRICANT". The FDA issued a decision of Substantially Equivalent on Apr 17, 2003. The device falls under product code HIS (Condom), a Class II device regulated under 21 CFR 884.5300. Suretex, Ltd. has 4 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 17, 2003
- Date Received
- Jan 17, 2003
- 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
- 510(k)