Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Gerard Medical Enterprises, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K954258	TRIMPORT IMPLANTABLE ACCESS SYSTEM (MODIFICATION)	LJT	1996-05-24	View
510(k)	K945250	TRIMPORT	LJT	1995-03-07	View
510(k)	K942623	TRIMPORT	LJT	1994-08-23	View
510(k)	K922147	DUAL PLASTIC VASCULAR ACCESS SYSTEM	LJT	1992-12-04	View
510(k)	K913114	TRIM-PORT(TM) IMPLANT ACCESS SYST DUAL TITAN PORT	FMF	1992-01-02	View
510(k)	K912111	MODIFIED VERSION IMPLANTABLE VASCULAR ACCESS SYSTE	FMF	1991-10-08	View
510(k)	K903364	GERARD MEDICAL, INC. TRIM-PORT	LJT	1990-10-31	View
510(k)	K813358	GERARD MEDICAL ELECTRODE TESTER	KRC	1981-12-29	View

↑