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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 K802311
Device Name MO8 OXYGEN FLOWMETER
Applicant
TIMETER INSTRUMENT CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
TIMETER INSTRUMENT CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.2340
Classification Product Code
CAX  
Date Received09/23/1980
Decision Date 10/23/1980
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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