P51 ANGIOPLASTY PRESSURE TRANSDUCER

P51 ANGIOPLASTY PRESSURE TRANSDUCER is an FDA 510(k)-cleared medical device (K813331) manufactured by Konigsberg Instruments, 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 December 28, 1981. Regulation: 8.