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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Rhinoanemometer (Measurement Of Nasal Decongestion)
510(k) Number K853024
Device Name RHINOTEST MP
Applicant
Intertronic, Inc.
7707 E. Acoma
Suite 113
Scottsdale,  AZ  85260
Applicant Contact K. R MERILLAT
Correspondent
Intertronic, Inc.
7707 E. Acoma
Suite 113
Scottsdale,  AZ  85260
Correspondent Contact K. R MERILLAT
Regulation Number868.1800
Classification Product Code
BXQ  
Date Received07/18/1985
Decision Date 09/27/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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