FDA 510(k) Application Details - K991072

Device Classification Name Implant, Eye Valve

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510(K) Number K991072
Device Name Implant, Eye Valve
Applicant NEW WORLD MEDICAL, INC.
10763 EDISON CT.
RANCHO CUCAMONGA, CA 91730 US
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Contact A.M. AHMED
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Regulation Number 886.3920

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Classification Product Code KYF
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Date Received 03/31/1999
Decision Date 07/13/1999
Decision SESE - SUBST EQUIV
Classification Advisory Committee OP - Ophthalmic
Review Advisory Committee OP - Ophthalmic
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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