LASERPOR AP ATRIAL ENDOCARD. ELECTR. LD.

LASERPOR AP ATRIAL ENDOCARD. ELECTR. LD. is an FDA 510(k)-cleared medical device (K820121) manufactured by Telectronics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on February 11, 1982. Regulation: 8.