
Cardiac Mariners, Inc.
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VASCO SCANNING BEAM DIGITAL X-RAY SYSTEM is an FDA 510(k)-cleared medical device (K982345) manufactured by Cardiac Mariners, 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 August 31, 1998. Regulation: 8.

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