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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name oximeter
510(k) Number K874198
Device Name VITALOG HMS-3000
Applicant
VITALOG CORP.
643 BAIR ISLAND RD.
SUITE 300
REDWOOD,  CA  94063
Applicant Contact BRUCE RULE
Correspondent
VITALOG CORP.
643 BAIR ISLAND RD.
SUITE 300
REDWOOD,  CA  94063
Correspondent Contact BRUCE RULE
Regulation Number870.2700
Classification Product Code
DQA  
Date Received10/09/1987
Decision Date 03/22/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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