PHICAL TEST— 510(k) DEN060001

Unknown

Genova Diagnostics

FDA 510(k) clearance DEN060001 for PHICAL TEST, Unknown on 2006-04-26. Applicant: Genova Diagnostics. Device class: 2.

Clearance details

Applicant: Genova Diagnostics
Product code: Code NXO
Device class: Class 2
Regulation: 21 CFR 866.5180
Advisory panel: Immunology
Date received: 2006-03-23
Decision date: 2006-04-26
Decision: Unknown
Clearance type: Post-NSE
Location: Asheville, NC, US

View on FDA.gov ↗

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