Siemens Medical Solutions USA, Inc.
MODIFICATION TO MAGNETOM RHAPSODY SYSTEM
SKU K020573UPC LNH
In Stock
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IIFDA 510(k) Cleared (K020573)
1
Free shipping on orders over $99 · 30-day returns
Siemens Medical Solutions USA, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO MAGNETOM RHAPSODY SYSTEM is an FDA 510(k)-cleared medical device (K020573) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 2002. Regulation: 8.
