ClearanceBrief
Company ยท US

Summit Technology, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1998. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EQHSource, Carrier, Fiberoptic Light2
GEXPowered Laser Surgical Instrument1
HNOKeratome, Ac-Powered1
HQFLaser, Ophthalmic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 22, 1998K980675SUMMIT KRUMEICH-BARRAQUER MICROKERATOME
Summit Technology, Inc.
HNO
Jul 22, 1993K926470LASER AND EMPHASIS SCLEROSTOMY TIP
Summit Technology, Inc.
HQF
Jun 15, 1992K915651OMNIMED HOLMIUM LASER AND DELIVERY SYSTEM
Summit Technology, Inc.
GEX
Jul 25, 1991K912522OMNIVIEW(TM) OPHTHALMIC FIBERENDO W/NEEDLEHOLDER
Summit Technology, Inc.
EQH
Dec 24, 1990K904470SUMMIT TECH 19/20 GAUGE OPHTHALMIC FIBERENDOSCOPE
Summit Technology, Inc.
EQH

Latest recalls

DateFirm and productCodeLinked 510(k)
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