VIDA 55 PULSE-ECHO ULTRASONIC DEVICE— 510(k) K802279

Name: FDA 510(k) clearance K802279
Creator: U.S. Food and Drug Administration
Published: 1980-12-15

Substantially Equivalent

Vida, Inc.

FDA 510(k) clearance K802279 for VIDA 55 PULSE-ECHO ULTRASONIC DEVICE, Substantially Equivalent on 1980-12-15. Applicant: Vida, Inc.. Device class: 2.

Clearance details

Applicant: Vida, Inc.
Product code: Code EWG
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1980-09-18
Decision date: 1980-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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