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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K828605
Device Name BEAM LIMITING DEVICE
Applicant
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123
Correspondent
Rinn Corp.
1212 Abbott Dr.
Elgin,  IL  60123
Date Received11/29/1982
Decision Date 01/03/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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