MKS BEAM OUTLINE PROJECTOR— 510(k) K921876

Name: FDA 510(k) clearance K921876
Creator: U.S. Food and Drug Administration
Published: 1992-06-25

Substantially Equivalent

Medical Knowledge Systems, Inc.

FDA 510(k) clearance K921876 for MKS BEAM OUTLINE PROJECTOR, Substantially Equivalent on 1992-06-25. Applicant: Medical Knowledge Systems, Inc.. Device class: 2.

Clearance details

Applicant: Medical Knowledge Systems, Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1992-04-20
Decision date: 1992-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Detroit, MI, US

Download summary PDF View on FDA.gov ↗

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