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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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