CLINICAL ACQUISITION MODULE— 510(k) K780971

Name: FDA 510(k) clearance K780971
Creator: U.S. Food and Drug Administration
Published: 1978-06-22

Substantially Equivalent

Analytical Development Assoc. Corp.

FDA 510(k) clearance K780971 for CLINICAL ACQUISITION MODULE, Substantially Equivalent on 1978-06-22. Applicant: Analytical Development Assoc. Corp.. Device class: 1.

Clearance details

Applicant: Analytical Development Assoc. Corp.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 1978-06-12
Decision date: 1978-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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