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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Handpiece, Direct Drive, Ac-Powered
510(k) Number K813348
Device Name YOSHIDA RIDO-F, MODEL LM-01
Applicant
Kaycor Intl., Ltd.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Kaycor Intl., Ltd.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number872.4200
Classification Product Code
EKX  
Date Received11/27/1981
Decision Date 01/07/1982
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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