VYSIS AUTOVYSION SYSTEM— 510(k) DEN040010

Unknown

Vysis

FDA 510(k) clearance DEN040010 for VYSIS AUTOVYSION SYSTEM, Unknown on 2004-12-13. Applicant: Vysis. Device class: 2.

Clearance details

Applicant: Vysis
Product code: Code NTH
Device class: Class 2
Regulation: 21 CFR 866.4700
Advisory panel: Immunology
Date received: 2004-10-13
Decision date: 2004-12-13
Decision: Unknown
Clearance type: Post-NSE
Location: Downers Grove, IL, US

View on FDA.gov ↗

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