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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name light, ultraviolet, dermatological
510(k) Number K812446
Device Name SUNLAMP
Applicant
THE RICHMOND LIGHT CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
THE RICHMOND LIGHT CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4630
Classification Product Code
FTC  
Date Received08/28/1981
Decision Date 10/13/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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