Micro Link Endoscopic Fiber Cable, Model B1-90159

FDA 510(k) K001698 · Cogent Light Technologies, Inc.

Substantially Equivalent

510(k) numberK001698

Submission

Device name
Micro Link Endoscopic Fiber Cable, Model B1-90159
Applicant
Cogent Light Technologies, Inc.
Valencia, CA, US
Received
June 2, 2000
Decision date
July 17, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FFS – Image, Illumination, Fiberoptic, For Endoscope
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

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K023633Sovis Optique's Endoscopic CableFFS · Traditional Sovis Optique12/31/2002SE
K994084Smith & Nephew Xenon Light Sources and AccessoriesFFS · Traditional Smith & Nephew, Inc.01/20/2000SE
K991323Smith & Nephew Subcutaneous IlluminatorFFS · Traditional Smith & Nephew, Inc.07/06/1999SE
K983714Solartec Source 270, Model # 90123FFS · Traditional Cogent Light Technologies, Inc.12/23/1998SE
K982462Fiber Optic Endoillumination ProbeFFS · Traditional Microvision, Inc.09/14/1998SE
K980636Fiber Optic Endoillumination ProbeFFS · Traditional Dutch Ophthalmic USA, Inc.05/20/1998SE

More from Dutch Ophthalmic USA, Inc.

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K983714Solartec Source 270, Model # 90123FFS · Traditional 12/23/1998SE
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Questions and answers

When was Micro Link Endoscopic Fiber Cable, Model B1-90159 cleared by the FDA?

Micro Link Endoscopic Fiber Cable, Model B1-90159 (K001698) received a 510(k) decision of Substantially Equivalent on July 17, 2000, 45 days after the submission was received.

What is the product code of K001698?

The FDA product code is FFS – Image, Illumination, Fiberoptic, For Endoscope , a Class II (moderate risk) device regulated under 21 CFR 876.1500.