FOCUS— 510(k) K001729

Substantially Equivalent

Instrumentarium Corp.

FDA 510(k) clearance K001729 for FOCUS, Substantially Equivalent on 2000-07-13. Applicant: Instrumentarium Corp.. Device class: 2.

Clearance details

Applicant: Instrumentarium Corp.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2000-06-07
Decision date: 2000-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, 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.