FDA 510(k) Applications Submitted by KEN BLAKE

FDA 510(k) Number Submission Date Device Name Applicant
K960372 01/26/1996 SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM SCANLAN INTL., INC.
K081640 06/11/2008 GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS GIMMI GMBH
K092421 08/07/2009 ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTIC GIMMI GMBH


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