OUTPUT DIGITAL DISPLAY MODULE, MODEL 401— 510(k) K780356

Name: FDA 510(k) clearance K780356
Creator: U.S. Food and Drug Administration
Published: 1978-05-31

Substantially Equivalent

Output, Inc.

FDA 510(k) clearance K780356 for OUTPUT DIGITAL DISPLAY MODULE, MODEL 401, Substantially Equivalent on 1978-05-31. Applicant: Output, Inc.. Device class: 2.

Clearance details

Applicant: Output, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1978-03-06
Decision date: 1978-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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