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MS X-RAY GRID
MITAYA MANUFACTURING CO., LTD. · Model GMSBK06120040C0001 · UDI-DI 04589744211348
10
510(k) clearances
2
Adverse events
1
Recalls
20
Facilities
Description
460x460mm, 6:1,120cm, 40L/cm, CAP
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-08 | Eastman Kodak Co | Screens may be affected with image artifacts |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
