STEREOTIX— 510(k) K873618

Substantially Equivalent

Thomson-Cgr Medical Corp.

FDA 510(k) clearance K873618 for STEREOTIX, Substantially Equivalent on 1987-11-16. Applicant: Thomson-Cgr Medical Corp.. Device class: 2.

Clearance details

Applicant: Thomson-Cgr Medical Corp.
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1987-09-08
Decision date: 1987-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, 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.