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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K790352
Device Name NEPHROSS 11F100
Applicant
Redy Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Redy Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Date Received02/22/1979
Decision Date 02/22/1979
Decision SE - Postmarket Surveillance Required (SESP)
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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