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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K837515
Device Name DENTAL CASSETTE HOLDERS
Applicant
Xre Corp.
300 Foster St.
Littleton,  MA  01460
Correspondent
Xre Corp.
300 Foster St.
Littleton,  MA  01460
Date Received04/26/1983
Decision Date 06/28/1983
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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