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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 K870621
Device Name SATLITE/PB251 PULSE OXIMETER
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
P.O. BOX 446
SF-00101
HELSINKI, FINLAND,  FI
Applicant Contact HANNU AHJOPALO
Correspondent
DATEX DIVISION INSTRUMENTARIUM CORP.
P.O. BOX 446
SF-00101
HELSINKI, FINLAND,  FI
Correspondent Contact HANNU AHJOPALO
Regulation Number870.2700
Classification Product Code
DQA  
Date Received02/12/1987
Decision Date 03/20/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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