DIGITAL RADIATION DETECTOR— 510(k) K771301

Substantially Equivalent

Actus, Inc.

FDA 510(k) clearance K771301 for DIGITAL RADIATION DETECTOR, Substantially Equivalent on 1977-08-04. Applicant: Actus, Inc.. Device class: 1.

Clearance details

Applicant: Actus, Inc.
Product code: Code IZD
Device class: Class 1
Regulation: 21 CFR 892.1320
Advisory panel: Radiology
Date received: 1977-07-15
Decision date: 1977-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.