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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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