
Berman, Pcp & Consultants, Inc.
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INFUSION SET TYPE S is an FDA 510(k)-cleared medical device (K771267) manufactured by Berman, Pcp & Consultants, 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 September 11, 1977. Regulation: 8.

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