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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 K944608
Device Name HP M1722A/B AND M1723A/B CODEMASTER
Applicant
Hewlett-Packard Co.
1700 S. Baker St.
Mcminnville,  OR  97128
Applicant Contact NANCY WINN
Correspondent
Hewlett-Packard Co.
1700 S. Baker St.
Mcminnville,  OR  97128
Correspondent Contact NANCY WINN
Regulation Number870.2700
Classification Product Code
DQA  
Date Received09/19/1994
Decision Date 10/04/1994
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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