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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Needle, Hypodermic, Single Lumen
510(k) Number K913885
Device Name RINN E-Z CAPPER
Applicant
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123
Applicant Contact RAYMOND G JACOBS
Correspondent
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123
Correspondent Contact RAYMOND G JACOBS
Regulation Number880.5570
Classification Product Code
FMI  
Date Received08/29/1991
Decision Date 12/13/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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