ANEUVYSION— 510(k) K972200

Substantially Equivalent

Vysis

FDA 510(k) clearance K972200 for ANEUVYSION, Substantially Equivalent on 1997-10-20. Applicant: Vysis.

Clearance details

Applicant
Vysis
Product code
Code OYU
Advisory panel
Immunology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Downers Grove, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.