ARCHIVEMANAGER— 510(k) K950513

Substantially Equivalent

Cemax, Inc.

FDA 510(k) clearance K950513 for ARCHIVEMANAGER, Substantially Equivalent on 1995-11-13. Applicant: Cemax, Inc.. Device class: 1.

Clearance details

Applicant
Cemax, Inc.
Product code
Code LMD
Device class
Class 1
Regulation
21 CFR 892.2020
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Fremont, CA, US
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