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.

Summit Technology, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K980675	SUMMIT KRUMEICH-BARRAQUER MICROKERATOME	HNO	1998-12-22	View
510(k)	K926470	LASER AND EMPHASIS SCLEROSTOMY TIP	HQF	1993-07-22	View
510(k)	K915651	OMNIMED HOLMIUM LASER AND DELIVERY SYSTEM	GEX	1992-06-15	View
510(k)	K912522	OMNIVIEW(TM) OPHTHALMIC FIBERENDO W/NEEDLEHOLDER	EQH	1991-07-25	View
510(k)	K904470	SUMMIT TECH 19/20 GAUGE OPHTHALMIC FIBERENDOSCOPE	EQH	1990-12-24	View

↑