K963319Substantially Equivalent
Olympus,jasmine,jimmy-O Raincoat,drink,ares,aphrodit,zeus,apollo,selfcare,careplus,titan
Custom Services Intl., Inc., Las Vegas NV / Traditional, Substantially Equivalent
K963319 is the FDA 510(k) clearance record for OLYMPUS,JASMINE,JIMMY-O RAINCOAT,DRINK,ARES,APHRODIT,ZEUS,APOLLO,SELFCARE,CAREPLUS,TITAN, a class II device, cleared for Custom Services Intl., Inc. on under FDA product code HIS (Condom). FDA records list 9 510(k) clearances for Custom Services Intl., Inc., from to . As of , FDA records show no recalls naming K963319.
Clearance record
- Decision date
- Received
- (163 days to decision)
- Product code
- HIS Condom
- Regulation
- 21 CFR 884.5300
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Custom Services Intl., Inc. 3111 W. Post Rd., Las Vegas NV
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code HIS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
