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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Light, Operating, Dental
510(k) Number K926081
Device Name DENTAL LIGHT
Applicant
Mdt Corp., Inc.
1777 E. Henrietta Rd.(14623)
P.O. Box 23077
Rochester,  NY  14692
Applicant Contact MARK N SMITH
Correspondent
Mdt Corp., Inc.
1777 E. Henrietta Rd.(14623)
P.O. Box 23077
Rochester,  NY  14692
Correspondent Contact MARK N SMITH
Regulation Number872.4630
Classification Product Code
EAZ  
Date Received12/01/1992
Decision Date 01/26/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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