SCANDIPLAN - VERSION 338— 510(k) K914926

Substantially Equivalent

Scanditronix, Inc.

FDA 510(k) clearance K914926 for SCANDIPLAN - VERSION 338, Substantially Equivalent on 1992-05-28. Applicant: Scanditronix, Inc.. Device class: 2.

Clearance details

Applicant: Scanditronix, Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1991-11-04
Decision date: 1992-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Essex, MA, US

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