K062586Substantially Equivalent
Xplorer 1600 Plus
Imaging Dynamics Company, Ltd., Calgary, Alberta, CA / Special, Substantially Equivalent
K062586 is the FDA 510(k) clearance record for XPLORER 1600 PLUS, a class II device, cleared for Imaging Dynamics Company , Ltd. on under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)). FDA records list 21 510(k) clearances for Imaging Dynamics Company , Ltd., from to . As of , FDA records show no recalls naming K062586.
Clearance record
- Decision date
- Received
- (28 days to decision)
- Product code
- MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
- Regulation
- 21 CFR 892.1680
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Imaging Dynamics Company , Ltd. 151,2340 Pegasus Way, NE, Calgary, Alberta, CA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code MQB
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 2 |
| July 2026 | 1 |
| August 2026 | 0 |
| 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.
