ZIKON 100 DIGITAL X-RAY SYSTEM— 510(k) K813032

Name: FDA 510(k) clearance K813032
Creator: U.S. Food and Drug Administration
Published: 1981-11-24

Substantially Equivalent

Kontron Instruments, Inc.

FDA 510(k) clearance K813032 for ZIKON 100 DIGITAL X-RAY SYSTEM, Substantially Equivalent on 1981-11-24. Applicant: Kontron Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Kontron Instruments, Inc.
Product code: Code JAB
Device class: Class 2
Regulation: 21 CFR 892.1660
Advisory panel: Radiology
Date received: 1981-10-28
Decision date: 1981-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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