K964167Substantially Equivalent
Decision Support System (for Radiation Oncology)
Multidata Systems International Corp., St. Louis MO / Traditional, Substantially Equivalent
K964167 is the FDA 510(k) clearance record for DECISION SUPPORT SYSTEM (FOR RADIATION ONCOLOGY), a class II device, cleared for Multidata Systems International Corp. on under FDA product code IYE (Accelerator, Linear, Medical). FDA records list one 510(k) clearance for Multidata Systems International Corp. As of , FDA records show one recall naming K964167.
Clearance record
- Decision date
- Received
- (156 days to decision)
- Product code
- IYE Accelerator, Linear, Medical
- Regulation
- 21 CFR 892.5050
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Multidata Systems International Corp. 9801 Manchester Rd., St. Louis MO
- 510(k) summary
- Statement
- 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 |
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