EASY MOVING PLUS, SM-XXHF-YY— 510(k) K090322
Substantially EquivalentSedecal., Sa.
FDA 510(k) clearance K090322 for EASY MOVING PLUS, SM-XXHF-YY, Substantially Equivalent on 2009-03-17. Applicant: Sedecal., Sa.. Device class: 2.
Clearance details
- Applicant
- Sedecal., Sa.
- Product code
- Code IZL
- Device class
- Class 2
- Regulation
- 21 CFR 892.1720
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Deerfield, IL, US
Recent devices under product code IZL
view allMore clearances from Sedecal., Sa.
view allAdverse events under product code IZL
product code IZL- Other
- 3
- Total
- 3
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K090322
K-number listed on FDA's recall record- Z-0253-2026 — Model Number 40KWMOBILE3.899, Mobile X-ray system
- Z-0254-2026 — Model Number SM-20HF-Batt; 20KW ANALOG, Mobile X-ray system
- Z-0255-2026 — Model Number SM-32HF-B-D-C; 32KW 50G, Mobile X-ray system
- Z-0256-2026 — Model SM-32HF-Batt; 32KW ANALOG, Mobile X-ray system
- Z-0257-2026 — Model SM-40HF-B-D-C; 40KW - CANON READY, Mobile X-ray system
- Z-0258-2026 — Model Number SM-40HF-B-D-C; 40KW 50G, Mobile X-ray system
- Z-0259-2026 — Model Number SM-40HF-B-D-C; 40KW 55C, Mobile X-ray system
- Z-0260-2026 — Model SM-40HF-B-D-C; 40KW 70C, Mobile X-ray system
- Z-0261-2026 — Model Number SM-40HF-Batt; 40KW ANALOG, Mobile X-ray system
- Z-0262-2026 — Sedecal Easy Moving Plus Model Number SM-50HF-B-D-C; 50KW 50G, Mobile X-ray system
- Z-0263-2026 — Model Number SM-40HF-B-D-C; 40KW 50C, Mobile X-ray system
- Z-0264-2026 — Model Number SM-40HF-B-D-C; 40KW 50G, Mobile X-ray system
- Z-0265-2026 — Model Number SM-40HF-B-D-C; 40KW 55C, Mobile X-ray system
- Z-0266-2026 — Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system
- Z-0267-2026 — Model Number SM-40HF-B-D-C; 40KW 55G, Mobile X-ray system
- Z-0268-2026 — Model Number SM-40HF-B-D-C; 40KW 55G/60G, Mobile X-ray system
- Z-0269-2026 — Model Number SM-40HF-B-D-C; 40KW 55C, Mobile X-ray system
- Z-0270-2026 — Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system
- Z-0271-2026 — Model Number SM-40HF-B-D-C; 40KW 70C, Mobile X-ray system
- Z-0272-2026 — Model Number SM-40HF-B-D-C; 40KW 70C EN, Mobile X-ray system
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K090322.
Data sourced from openFDA. This site is unofficial and independent of the FDA.