ZIRBLOCK— 510(k) K070537

Substantially Equivalent

Cdl Technologies, Inc.

FDA 510(k) clearance K070537 for ZIRBLOCK, Substantially Equivalent on 2007-04-30. Applicant: Cdl Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Cdl Technologies, Inc.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2007-02-26
Decision date: 2007-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, 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.