Jed-Light Fiberoptic Light Source

FDA 510(k) K954184 · Jedmed Instrument Co.

Substantially Equivalent

510(k) numberK954184

Submission

Device name
Jed-Light Fiberoptic Light Source
Applicant
Jedmed Instrument Co.
Saint Louis, MO, US
Received
September 6, 1995
Decision date
November 13, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EQH – Source, Carrier, Fiberoptic Light
Device class
Class I (low risk)
Regulation
21 CFR 874.4350
Specialty
Ear, Nose, Throat

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K932771Battery Powered, Disposable Endoscope Light SourceEQH · Traditional Xomed-Treace, Inc.08/24/1994SE
K941661GM Opti*Cam Camer with Dental Fiber Optic LightEQH · Traditional Gm Engineering, Inc.08/23/1994SE
K941662GM Opti*Cam Camera with ENT Fiber Optic LightEQH · Traditional Gm Engineering, Inc.07/20/1994SE
K934911Saphire Plus Surgical MirrorEQH · Traditional San Diego Swiss Machining, Inc.06/21/1994SE
K932131Mid Labs Twin IlluminatorEQH · Traditional Medical Instrument Development Laboratories, Inc.04/01/1994SE
K930123Aspirating Endo Ocular ProbeEQH · Traditional Surgical Technologies, Inc.02/16/1994SE
K933145Fiberoptic Lightsources and CarriersEQH · Traditional Electro Fiberoptics Corp.09/07/1993SE
K923227Throat-A-ScopeEQH · Traditional Truphatek, Ltd.12/04/1992SE

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Questions and answers

When was Jed-Light Fiberoptic Light Source cleared by the FDA?

Jed-Light Fiberoptic Light Source (K954184) received a 510(k) decision of Substantially Equivalent on November 13, 1995, 68 days after the submission was received.

What is the product code of K954184?

The FDA product code is EQH – Source, Carrier, Fiberoptic Light, a Class I (low risk) device regulated under 21 CFR 874.4350.