MAMMAPRINT— 510(k) DEN070009

Unknown

Agendia BV

FDA 510(k) clearance DEN070009 for MAMMAPRINT, Unknown on 2007-02-06. Applicant: Agendia BV. Device class: 2.

Clearance details

Applicant: Agendia BV
Product code: Code NYI
Device class: Class 2
Regulation: 21 CFR 866.6040
Advisory panel: Immunology
Date received: 2007-01-30
Decision date: 2007-02-06
Decision: Unknown
Clearance type: Post-NSE
Location: Amsterdam, NL

View on FDA.gov ↗

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