AUTOMATIC FILM PROCESSORIO M. R80— 510(k) K781068

Name: FDA 510(k) clearance K781068
Creator: U.S. Food and Drug Administration
Published: 1978-07-17

Substantially Equivalent

Tecnomed, Inc.

FDA 510(k) clearance K781068 for AUTOMATIC FILM PROCESSORIO M. R80, Substantially Equivalent on 1978-07-17. Applicant: Tecnomed, Inc.. Device class: 1.

Clearance details

Applicant: Tecnomed, Inc.
Product code: Code IWX
Device class: Class 1
Regulation: 21 CFR 892.6500
Advisory panel: Radiology
Date received: 1978-06-26
Decision date: 1978-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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