
D.R.O. Medical, Inc.
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FLOW MED SK 140 BURET is an FDA 510(k)-cleared medical device (K844820) manufactured by D.R.O. Medical, 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 January 27, 1985. Regulation: 8.

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