K960553Substantially Equivalent
Card Guard Model Cg-900
Card Guard Scientific Survival, Ltd., Malibu CA / Traditional, Substantially Equivalent
K960553 is the FDA 510(k) clearance record for CARD GUARD MODEL CG-900, a class II device, cleared for Card Guard Scientific Survival , Ltd. on under FDA product code HGM (System, Monitoring, Perinatal). FDA records list 49 510(k) clearances for Card Guard Scientific Survival , Ltd., from to . As of , FDA records show no recalls naming K960553.
Clearance record
- Decision date
- Received
- (439 days to decision)
- Product code
- HGM System, Monitoring, Perinatal
- Regulation
- 21 CFR 884.2740
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Card Guard Scientific Survival , Ltd. 3649 Sehorn Dr., Malibu CA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code HGM
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 0 |
| 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.
