M-2000 DIAGNOSTIC AND TELERADIOLOGY WORKSTATION— 510(k) K921278

Name: FDA 510(k) clearance K921278
Creator: U.S. Food and Drug Administration
Published: 1992-05-18

Substantially Equivalent

Metecon, Inc.

FDA 510(k) clearance K921278 for M-2000 DIAGNOSTIC AND TELERADIOLOGY WORKSTATION, Substantially Equivalent on 1992-05-18. Applicant: Metecon, Inc.. Device class: 1.

Clearance details

Applicant: Metecon, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1992-03-17
Decision date: 1992-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

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