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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laser, Ent Microsurgical Carbon-Dioxide
510(k) Number K802279
Device Name VIDA 55 PULSE-ECHO ULTRASONIC DEVICE
Applicant
VIDA, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
VIDA, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number874.4500
Classification Product Code
EWG  
Date Received09/18/1980
Decision Date 12/15/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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