D-SCOPE III— 510(k) K884661

Substantially Equivalent

Medx, Inc.

FDA 510(k) clearance K884661 for D-SCOPE III, Substantially Equivalent on 1989-04-12. Applicant: Medx, Inc.. Device class: 1.

Clearance details

Applicant: Medx, Inc.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 1988-11-07
Decision date: 1989-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

Download summary PDF View on FDA.gov ↗

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