IDXVIEW— 510(k) K954071

Substantially Equivalent

Idx Systems Corp.

FDA 510(k) clearance K954071 for IDXVIEW, Substantially Equivalent on 1996-02-27. Applicant: Idx Systems Corp.. Device class: 1.

Clearance details

Applicant: Idx Systems Corp.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1995-08-30
Decision date: 1996-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, VT, US

Download summary PDF View on FDA.gov ↗

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