ARRIPRO 35 ST/TV— 510(k) K973115

Substantially Equivalent

Arnold & Richter Cine Technik

FDA 510(k) clearance K973115 for ARRIPRO 35 ST/TV, Substantially Equivalent on 1997-09-02. Applicant: Arnold & Richter Cine Technik. Device class: 1.

Clearance details

Applicant: Arnold & Richter Cine Technik
Product code: Code IXC
Device class: Class 1
Regulation: 21 CFR 892.1890
Advisory panel: Radiology
Date received: 1997-08-20
Decision date: 1997-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Munich, DE

Download summary PDF View on FDA.gov ↗

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