DORC INTRAOCULAR ELECTROMAGNET— 510(k) K830336

Name: FDA 510(k) clearance K830336
Creator: U.S. Food and Drug Administration
Published: 1983-03-09

Substantially Equivalent

Jedmed Instrument Co.

FDA 510(k) clearance K830336 for DORC INTRAOCULAR ELECTROMAGNET, Substantially Equivalent on 1983-03-09. Applicant: Jedmed Instrument Co.. Device class: 2.

Clearance details

Applicant: Jedmed Instrument Co.
Product code: Code HPO
Device class: Class 2
Regulation: 21 CFR 886.4440
Advisory panel: Ophthalmic
Date received: 1983-02-01
Decision date: 1983-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.