510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K953902Substantially Equivalent

Giotto High Tech (H.t.) Mammographic System

Medical Marketing Intl., Inc., Baton Rouge LA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K953902 is the FDA 510(k) clearance record for GIOTTO HIGH TECH (H.T.) MAMMOGRAPHIC SYSTEM, a class II device, cleared for Medical Marketing Intl., Inc. on under FDA product code IZH (System, X-Ray, Mammographic). FDA records list one 510(k) clearance for Medical Marketing Intl., Inc. As of , FDA records show no recalls naming K953902.

Clearance record

Decision date
Received
(579 days to decision)
Product code
IZH System, X-Ray, Mammographic
Regulation
21 CFR 892.1710
Device class
Class II
Review panel
Radiology
Applicant
Medical Marketing Intl., Inc. 12748 E. Millburn Ave., Baton Rouge LA
510(k) summary
Statement
Third party review
No

Clearances, product code IZH

Trailing 12 months

FDA records hold no clearances under product code IZH in the trailing twelve months.

FDA records show no clearances under product code IZH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IZH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260