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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact