510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K201340Substantially Equivalent

Aquila 320 D / Aquila 320 S

Vmi Tecnologias Ltda, Aparecido De Oliveira, Lagoa Santa, BR / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K201340 is the FDA 510(k) clearance record for AQUILA 320 D / AQUILA 320 S, a class II device, cleared for Vmi Tecnologias Ltda on under FDA product code IZL (System, X-Ray, Mobile). FDA records list 3 510(k) clearances for Vmi Tecnologias Ltda, from to . As of , FDA records show no recalls naming K201340.

Clearance record

Decision date
Received
(30 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
Vmi Tecnologias Ltda Rua Prefeito Elizeu Alves Da Silva, 400 Dist. Ind. Genesco, Aparecido De Oliveira, Lagoa Santa, BR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IZL

Trailing 12 months
7 clearances under product code IZL in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code IZL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20261
July 20260
August 20261
September 20260
October 20261