JED-LIGHT FIBEROPTIC LIGHT SOURCE— 510(k) K954184

Name: FDA 510(k) clearance K954184
Creator: U.S. Food and Drug Administration
Published: 1995-11-13

Substantially Equivalent

Jedmed Instrument Co.

FDA 510(k) clearance K954184 for JED-LIGHT FIBEROPTIC LIGHT SOURCE, Substantially Equivalent on 1995-11-13. Applicant: Jedmed Instrument Co.. Device class: 1.

Clearance details

Applicant: Jedmed Instrument Co.
Product code: Code EQH
Device class: Class 1
Regulation: 21 CFR 874.4350
Advisory panel: Ear, Nose, Throat
Date received: 1995-09-06
Decision date: 1995-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Louis, MO, US

Download summary PDF View on FDA.gov ↗

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