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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Aid, Cardiopulmonary Resuscitation
510(k) Number K833737
Device Name CPR LOCATOR
Applicant
Lifepoint,Inc
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Lifepoint,Inc
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number870.5210
Classification Product Code
LIX  
Date Received10/25/1983
Decision Date 08/24/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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