Ion Beam Applications S.A.
MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235
SKU K101508UPC LHN
In Stock
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IIFDA 510(k) Cleared (K101508)
1
Free shipping on orders over $99 · 30-day returns
Ion Beam Applications S.A.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235 is an FDA 510(k)-cleared medical device (K101508) manufactured by Ion Beam Applications S.A.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 2010. Regulation: 8.
