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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name flowmeter, tube, thorpe, back-pressure compensated
510(k) Number K854067
Device Name SELECT FLOWMETER
Applicant
PRECISION MEDICAL, INC.
7285 PARK DR.
BATH,  PA  18014
Applicant Contact CLYDE W SHUMAN
Correspondent
PRECISION MEDICAL, INC.
7285 PARK DR.
BATH,  PA  18014
Correspondent Contact CLYDE W SHUMAN
Regulation Number868.2340
Classification Product Code
CAX  
Date Received10/04/1985
Decision Date 10/29/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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