COMPUMED DICON CLIENT— 510(k) K955708

Substantially Equivalent

Compumed, Inc.

FDA 510(k) clearance K955708 for COMPUMED DICON CLIENT, Substantially Equivalent on 1996-03-01. Applicant: Compumed, Inc.. Device class: 1.

Clearance details

Applicant: Compumed, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1995-12-14
Decision date: 1996-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Meeteetse, WY, US

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