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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, peritoneal, automatic delivery
510(k) Number K841929
Device Name LIFEMED LIFECOIL CATHETERS
Applicant
LIFEMED OF CALIFORNIA
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
LIFEMED OF CALIFORNIA
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number876.5630
Classification Product Code
FKX  
Date Received05/10/1984
Decision Date 08/08/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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