EMI SIMULATOR REMOTE CONTROL CONSOLE— 510(k) K781519

Name: FDA 510(k) clearance K781519
Creator: U.S. Food and Drug Administration
Published: 1978-09-14

Substantially Equivalent

Emi Medical, Inc.

FDA 510(k) clearance K781519 for EMI SIMULATOR REMOTE CONTROL CONSOLE, Substantially Equivalent on 1978-09-14. Applicant: Emi Medical, Inc.. Device class: 2.

Clearance details

Applicant: Emi Medical, Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1978-09-01
Decision date: 1978-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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