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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name collector, ostomy
510(k) Number K870577
Device Name E-Z LOOP
Applicant
JOHN F. GREER CO., INC.
530 E. 12TH ST.
OAKLAND,  CA  94606
Applicant Contact L. H GREER
Correspondent
JOHN F. GREER CO., INC.
530 E. 12TH ST.
OAKLAND,  CA  94606
Correspondent Contact L. H GREER
Regulation Number876.5900
Classification Product Code
EXB  
Date Received02/10/1987
Decision Date 04/17/1987
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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