MODULEX RTP SYSTEM— 510(k) K913017

Name: FDA 510(k) clearance K913017
Creator: U.S. Food and Drug Administration
Published: 1991-10-17

Substantially Equivalent

Computerized Medical Systems, Inc.

FDA 510(k) clearance K913017 for MODULEX RTP SYSTEM, Substantially Equivalent on 1991-10-17. Applicant: Computerized Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Computerized Medical Systems, Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1991-07-09
Decision date: 1991-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maryland Heights, MO, US

Download summary PDF View on FDA.gov ↗

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