GIOTTO HIGH TECH (H.T.) MAMMOGRAPHIC SYSTEM— 510(k) K953902

Name: FDA 510(k) clearance K953902
Creator: U.S. Food and Drug Administration
Published: 1997-03-19

Substantially Equivalent

Medical Marketing Intl., Inc.

FDA 510(k) clearance K953902 for GIOTTO HIGH TECH (H.T.) MAMMOGRAPHIC SYSTEM, Substantially Equivalent on 1997-03-19. Applicant: Medical Marketing Intl., Inc.. Device class: 2.

Clearance details

Applicant: Medical Marketing Intl., Inc.
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1995-08-18
Decision date: 1997-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baton Rouge, LA, 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.