
Solcoor, Inc.
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PEAK FLOWMETERS FOR SPIROMETRY is an FDA 510(k)-cleared medical device (K851265) manufactured by Solcoor, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 28, 1985. Regulation: 8.

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