
Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh
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S*E*M*M* SET FOR MOTO DRIVE WISAP #7689 SSM (MODIFICATION) is an FDA 510(k)-cleared medical device (K960640) manufactured by Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 13, 1997. Regulation: 8.

Ansell
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