PREMISE MODIFIED— 510(k) K090292

Substantially Equivalent

Kerr Corp.

FDA 510(k) clearance K090292 for PREMISE MODIFIED, Substantially Equivalent on 2009-04-03. Applicant: Kerr Corp.. Device class: 2.

Clearance details

Applicant: Kerr Corp.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2009-02-05
Decision date: 2009-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, CA, 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.