
Rd Medical Mfg., Inc.
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PARSET, MODEL A10001E is an FDA 510(k)-cleared medical device (K992104) manufactured by Rd Medical Mfg., Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 22, 1999. Regulation: 8.

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