KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263— 510(k) K862261

Name: FDA 510(k) clearance K862261
Creator: U.S. Food and Drug Administration
Published: 1987-02-19

Substantially Equivalent

Kontron Instruments, Inc.

FDA 510(k) clearance K862261 for KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263, Substantially Equivalent on 1987-02-19. Applicant: Kontron Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Kontron Instruments, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1986-06-13
Decision date: 1987-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Everett, MA, US

Download summary PDF View on FDA.gov ↗

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