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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Ear Wick
510(k) Number K920357
Device Name ULTRACELL EAR WICK
Applicant
ULTRACELL MEDICAL TECHNOLOGIES, INC.
P.O. BOX 326
NORTH STONINGTON,  CT  06359
Applicant Contact GEORGE P KORTEWEG
Correspondent
ULTRACELL MEDICAL TECHNOLOGIES, INC.
P.O. BOX 326
NORTH STONINGTON,  CT  06359
Correspondent Contact GEORGE P KORTEWEG
Regulation Number874.5220
Classification Product Code
KCN  
Date Received01/27/1992
Decision Date 02/01/1993
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
Recalls CDRH Recalls
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