PATHWORK DIAGNOSTICS TISSUE OF ORIGIN TEST— 510(k) K080896

Name: FDA 510(k) clearance K080896
Creator: U.S. Food and Drug Administration
Published: 2008-07-30

Unknown

Pathwork Diagnostics, Inc.

FDA 510(k) clearance K080896 for PATHWORK DIAGNOSTICS TISSUE OF ORIGIN TEST, Unknown on 2008-07-30. Applicant: Pathwork Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Pathwork Diagnostics, Inc.
Product code: Code OIW
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 2008-03-31
Decision date: 2008-07-30
Decision: Unknown
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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