GIOTTO HT— 510(k) K973856

Substantially Equivalent

Sitco, Inc.

FDA 510(k) clearance K973856 for GIOTTO HT, Substantially Equivalent on 1997-11-21. Applicant: Sitco, Inc.. Device class: 2.

Clearance details

Applicant: Sitco, Inc.
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1997-10-09
Decision date: 1997-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mundelein, 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.