ARTUS DRILL #3000— 510(k) K803290

Substantially Equivalent

Jedmed Instrument Co.

FDA 510(k) clearance K803290 for ARTUS DRILL #3000, Substantially Equivalent on 1981-01-28. Applicant: Jedmed Instrument Co.. Device class: 2.

Clearance details

Applicant: Jedmed Instrument Co.
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 1980-12-30
Decision date: 1981-01-28
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.