SCANSCOPE XT SYSTEM— 510(k) K071671

Substantially Equivalent

Aperio Technologies

FDA 510(k) clearance K071671 for SCANSCOPE XT SYSTEM, Substantially Equivalent on 2007-12-28. Applicant: Aperio Technologies. Device class: 2.

Clearance details

Applicant: Aperio Technologies
Product code: Code OEO
Device class: Class 2
Regulation: 21 CFR 864.1860
Advisory panel: Hematology
Date received: 2007-06-19
Decision date: 2007-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

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