INVIEW— 510(k) K051321

Substantially Equivalent

Metrika, Inc.

FDA 510(k) clearance K051321 for INVIEW, Substantially Equivalent on 2005-06-13. Applicant: Metrika, Inc.. Device class: 2.

Clearance details

Applicant: Metrika, Inc.
Product code: Code LCP
Device class: Class 2
Regulation: 21 CFR 864.7470
Advisory panel: Hematology
Date received: 2005-05-20
Decision date: 2005-06-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, 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.