K002039Substantially Equivalent
Ecat Pet Scanner, Models Ecat Exact and Ecat Exact Hr+ and Ecat Art
Siemens Medical Solutions USA, Inc., Knoxville TN / Traditional, Substantially Equivalent
K002039 is the FDA 510(k) clearance record for ECAT PET SCANNER, MODELS ECAT EXACT AND ECAT EXACT HR+ AND ECAT ART, a class II device, cleared for Cti Pet Systems, Inc. on under FDA product code LLZ (System, Image Processing, Radiological). FDA records list 829 510(k) clearances for SIEMENS MEDICAL SOLUTIONS USA, INC., from to . As of , FDA records show no recalls naming K002039.
Clearance record
- Decision date
- Received
- (84 days to decision)
- Product code
- LLZ System, Image Processing, Radiological
- Regulation
- 21 CFR 892.2050
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Cti Pet Systems, Inc. 810 Innovation Dr., Knoxville TN
- 510(k) summary
- Summary
- Third party review
- No
Clearances, product code LLZ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| December 2025 | 1 |
| January 2026 | 3 |
| February 2026 | 4 |
| March 2026 | 6 |
| April 2026 | 2 |
| May 2026 | 5 |
| June 2026 | 5 |
| July 2026 | 8 |
| August 2026 | 3 |
| September 2026 | 7 |
| October 2026 | 2 |
| November 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.
