PREFTEST PROFESSIONAL SUITE— 510(k) K052929

Name: FDA 510(k) clearance K052929
Creator: U.S. Food and Drug Administration
Published: 2006-04-26

Substantially Equivalent

Limestone Technologies, Inc.

FDA 510(k) clearance K052929 for PREFTEST PROFESSIONAL SUITE, Substantially Equivalent on 2006-04-26. Applicant: Limestone Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Limestone Technologies, Inc.
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 2005-10-19
Decision date: 2006-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dundas, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.