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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
Applicant Contact RAYMOND JACOBS
Correspondent
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123
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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