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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Collimator, Manual, Radiographic
510(k) Number K932134
Device Name RINN UNIVERSAL COLLIMATOR
Applicant
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123 -1819
Applicant Contact RAYMOND JACOBS
Correspondent
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123 -1819
Correspondent Contact RAYMOND JACOBS
Regulation Number892.1610
Classification Product Code
IZX  
Date Received05/03/1993
Decision Date 07/26/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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