
Rowenta, Inc.
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ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620) is an FDA 510(k)-cleared medical device (K023429) manufactured by Rowenta, 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 September 22, 2003. Regulation: 8.

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