
Rigel Medical Electronics, Inc.
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ECG PATIENT MONITOR 302 is an FDA 510(k)-cleared medical device (K850155) manufactured by Rigel Medical Electronics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 1985. Regulation: 8.

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