KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265— 510(k) K870815

Name: FDA 510(k) clearance K870815
Creator: U.S. Food and Drug Administration
Published: 1988-02-01

Substantially Equivalent

Kontron Instruments, Inc.

FDA 510(k) clearance K870815 for KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265, Substantially Equivalent on 1988-02-01. Applicant: Kontron Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Kontron Instruments, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1987-03-03
Decision date: 1988-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Everett, MA, US

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