K132064Substantially Equivalent
Biomarc Fiducial Marker
Carbon Medical Technologies, Inc., St. Paul MN / Traditional, Substantially Equivalent
K132064 is the FDA 510(k) clearance record for BIOMARC FIDUCIAL MARKER, a class II device, cleared for Carbon Medical Technologies, Inc. on under FDA product code IYE (Accelerator, Linear, Medical). FDA records list 18 510(k) clearances for Carbon Medical Technologies, Inc., from to . As of , FDA records show one recall naming K132064.
Clearance record
- Decision date
- Received
- (240 days to decision)
- Product code
- IYE Accelerator, Linear, Medical
- Regulation
- 21 CFR 892.5050
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Carbon Medical Technologies, Inc. 1290 Hammond Rd., St. Paul MN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code IYE
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 1 |
| January 2026 | 4 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 2 |
| May 2026 | 1 |
| June 2026 | 2 |
| July 2026 | 0 |
| August 2026 | 3 |
| 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.
