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FDA 510(k) Applications Submitted by Gloria Kolb
FDA 510(k) Number
Submission Date
Device Name
Applicant
K021140
04/09/2002
FOSSA EXPANDING DOUBLE PIGTAIL URETERAL STENT
FOSSA INDUSTRIES, INC.
K072293
08/16/2007
FOSSA URETERAL OPEN STENTS
FOSSA MEDICAL, INC.
K033368
10/21/2003
FOSSA URETERAL OPEN LUMEN STENT
FOSSA MEDICAL, INC.
K183585
12/21/2018
Elitone Device
Elidah, Inc.
K223884
12/27/2022
ELITONE Urge Urinary Incontinence Device
Elidah Inc
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