510(k) K972430
K972430 is an FDA 510(k) premarket notification submitted by Custom Services Intl., Inc. for the device "EXTRAWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9". The FDA issued a decision of Substantially Equivalent on September 10, 1997. The device falls under product code LTZ (Condom With Nonoxynol-9), a Class II device regulated under 21 CFR 884.5310. Custom Services Intl., Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 10, 1997
- Date Received
- June 27, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Condom With Nonoxynol-9
- Device Class
- Class II
- Regulation Number
- 884.5310
- Review Panel
- OB
- Submission Type