K244054Substantially Equivalent
16ch Flex SPEEDER Medium 1.5T (Q7000246); 16ch Flex SPEEDER Large 1.5T (Q7000247)
Quality Electrodynamics, Mayfield Village OH / Traditional, Substantially Equivalent
K244054 is the FDA 510(k) clearance record for 16ch Flex SPEEDER Medium 1.5T (Q7000246); 16ch Flex SPEEDER Large 1.5T (Q7000247), a class II device, cleared for Quality Electrodynamics on under FDA product code MOS (Coil, Magnetic Resonance, Specialty). FDA records list 34 510(k) clearances for Quality Electrodynamics, from to . As of , FDA records show no recalls naming K244054.
Clearance record
- Decision date
- Received
- (59 days to decision)
- Product code
- MOS Coil, Magnetic Resonance, Specialty
- Regulation
- 21 CFR 892.1000
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Quality Electrodynamics 6655 Beta Dr., Mayfield Village OH
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code MOS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 2 |
| February 2026 | 1 |
| March 2026 | 1 |
| April 2026 | 3 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 2 |
| 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.
