
Scientific Pharmaceuticals, Inc.
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PRELUDE (TEMPORARY CROWN AND BRIDGE CEMENT) is an FDA 510(k)-cleared medical device (K901077) manufactured by Scientific Pharmaceuticals, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 28, 1990. Regulation: 8.