TELESCOPING PENEVAC (MODIFICATION)

TELESCOPING PENEVAC (MODIFICATION) is an FDA 510(k)-cleared medical device (K961616) manufactured by I.C Medical, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 27, 1996. Regulation: 8.