FDA 510(k) Applications Submitted by DON HAAR

FDA 510(k) Number Submission Date Device Name Applicant
K980849 02/05/1998 SURGIN KIT SURGIN SURGICAL INSTRUMENTATION, INC.
K011195 04/19/2001 PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK; PRIZM BLADE (MORIA MODEL) CB / MK8511CB SURGIN SURGICAL INSTRUMENTATION, INC.
K033182 10/01/2003 PRIZM KERATOME BLADE (B.D. MODEL), MODEL MK8530BD SURGIN SURGICAL INSTRUMENTATION, INC.
K033236 10/06/2003 PRIZM KERATOME BLADE, MODEL MK8512M2 SURGIN SURGICAL INSTRUMENTATION, INC.
K013337 10/09/2001 PRIZM KERATOME BLADE (NIDEK MODEL), MODEL MK8514NI SURGIN INC


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