COLOR DOPPLER OPTION TO AI 5200 DIAG ULTRASO SYST— 510(k) K910212

Name: FDA 510(k) clearance K910212
Creator: U.S. Food and Drug Administration
Published: 1991-07-11

Substantially Equivalent

Acoustic Imaging Technologies Corp.

FDA 510(k) clearance K910212 for COLOR DOPPLER OPTION TO AI 5200 DIAG ULTRASO SYST, Substantially Equivalent on 1991-07-11. Applicant: Acoustic Imaging Technologies Corp.. Device class: 1.

Clearance details

Applicant: Acoustic Imaging Technologies Corp.
Product code: Code JYO
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1991-01-15
Decision date: 1991-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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