
Datascope Corp.
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PECOR 8.5 FRENCH IAB ON A DATASCOPE is an FDA 510(k)-cleared medical device (K831307) manufactured by Datascope Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 1, 1983. Regulation: 8.

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