ClearanceBrief
Company ยท US

Cogent Light Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2000. 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
FFSImage, Illumination, Fiberoptic, For Endoscope2
GCTLight Source, Endoscope, Xenon Arc2
FSTLight, Surgical, Fiberoptic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 17, 2000K001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159
Cogent Light Technologies, Inc.
FFS
Dec 23, 1998K983714SOLARTEC SOURCE 270, MODEL # 90123
Cogent Light Technologies, Inc.
FFS
Mar 28, 1997K971057COGENLIGHT TECHNOLOGIES XLS ILLUMINATOR SYSTEM
Cogent Light Technologies, Inc.
GCT
Mar 10, 1994K936048LIGHTWEAR(TM) SYST (LIGHTWEAR HEADLIGHT CLIP/HEADBAND)
Cogent Light Technologies, Inc.
FST
Feb 18, 1994K933405COGENT LIGHT ILLUMINATOR 10010 XENON LIGHT SOURCE
Cogent Light Technologies, Inc.
GCT

Latest recalls

DateFirm and productCodeLinked 510(k)
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