MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM— 510(k) K003090

Name: FDA 510(k) clearance K003090
Creator: U.S. Food and Drug Administration
Published: 2000-10-18

Substantially Equivalent

Midmark Corp.

FDA 510(k) clearance K003090 for MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM, Substantially Equivalent on 2000-10-18. Applicant: Midmark Corp.. Device class: 1.

Clearance details

Applicant: Midmark Corp.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2000-10-03
Decision date: 2000-10-18
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Versailles, OH, 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.