K100402Substantially Equivalent
Site-Rite Vision Ultrasound System
Bard Access Systems, Inc., Salt Lake Ciy, UT / Traditional, Substantially Equivalent
K100402 is the FDA 510(k) clearance record for SITE-RITE VISION ULTRASOUND SYSTEM, a class II device, cleared for Bard Access Systems, Inc. on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list 31 510(k) clearances for Bard Access Systems, Inc., from to . As of , FDA records show one recall naming K100402.
Clearance record
- Decision date
- Received
- (17 days to decision)
- Product code
- IYN System, Imaging, Pulsed Doppler, Ultrasonic
- Regulation
- 21 CFR 892.1550
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Bard Access Systems, Inc. 605 N. 5600 W., Salt Lake Ciy, UT
- 510(k) summary
- Summary PDF
- Third party review
- Yes
Clearances, product code IYN
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 6 |
| December 2025 | 6 |
| January 2026 | 4 |
| February 2026 | 1 |
| March 2026 | 6 |
| April 2026 | 3 |
| May 2026 | 11 |
| June 2026 | 3 |
| July 2026 | 6 |
| August 2026 | 3 |
| September 2026 | 3 |
| 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.
