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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 K871452
Device Name CLASSIC (TM) 200 OXYGEN FLOWMETER
Applicant
THE TIMETER GROUP
2501 OREGON PIKE
LANCASTER,  PA  17601
Applicant Contact TERRY L LANDIS
Correspondent
THE TIMETER GROUP
2501 OREGON PIKE
LANCASTER,  PA  17601
Correspondent Contact TERRY L LANDIS
Regulation Number868.2340
Classification Product Code
CAX  
Date Received04/13/1987
Decision Date 06/22/1987
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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