DU PONT LINX LASER IMAGER W/THE LINX NETWORKING— 510(k) K900935

Substantially Equivalent

E.I. Dupont DE Nemours & Co., Inc.

FDA 510(k) clearance K900935 for DU PONT LINX LASER IMAGER W/THE LINX NETWORKING, Substantially Equivalent on 1990-05-15. Applicant: E.I. Dupont DE Nemours & Co., Inc..

Clearance details

Applicant: E.I. Dupont DE Nemours & Co., Inc.
Product code: Code LMD
Advisory panel: Radiology
Date received: 1990-02-28
Decision date: 1990-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

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