STORZ DP4101 BASIC I/A PACK

STORZ DP4101 BASIC I/A PACK is an FDA 510(k)-cleared medical device (K953078) manufactured by Storz Instrument Co.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 6, 1995. Regulation: 8.