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

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..

Clearance details

Applicant: Vida, Inc.
Product code: Code EWG
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

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.