FIBEROPTIC LIGHTSOURCES AND CARRIERS— 510(k) K933145

Name: FDA 510(k) clearance K933145
Creator: U.S. Food and Drug Administration
Published: 1993-09-07

Substantially Equivalent

Electro Fiberoptics Corp.

FDA 510(k) clearance K933145 for FIBEROPTIC LIGHTSOURCES AND CARRIERS, Substantially Equivalent on 1993-09-07. Applicant: Electro Fiberoptics Corp.. Device class: 1.

Clearance details

Applicant: Electro Fiberoptics Corp.
Product code: Code EQH
Device class: Class 1
Regulation: 21 CFR 874.4350
Advisory panel: Ear, Nose, Throat
Date received: 1993-06-28
Decision date: 1993-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northborough, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EQH

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K945876 — WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT1995-12-04
K954184 — JED-LIGHT FIBEROPTIC LIGHT SOURCE1995-11-13
K951829 — COLD LIGHT SOURCE LOS 1501995-07-10
K932771 — BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCE1994-08-24
K941661 — GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT1994-08-23

More clearances from Electro Fiberoptics Corp.

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K943628 — ARTHROSCOPE1994-11-22
K921918 — FIBER OPTIC ENDOSCOPE1993-08-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.