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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Recorder, External, Pressure, Amplifier & Transducer
510(k) Number K801757
Device Name MMI/GAELTEC CATHETER TIP PRESS. TRANSDU
Applicant
MEDICAL MEASUREMENTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MEDICAL MEASUREMENTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.1725
Classification Product Code
FES  
Date Received07/28/1980
Decision Date 08/27/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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