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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Gauge, Depth, Instrument, Dental
510(k) Number K872215
Device Name PERIO-TEST
Applicant
Dr. Bernard Loewenthal
278 Lafayette Rd.
Portsmouth,  NH  03801
Applicant Contact BERNARD LOEWENTHAL
Correspondent
Dr. Bernard Loewenthal
278 Lafayette Rd.
Portsmouth,  NH  03801
Correspondent Contact BERNARD LOEWENTHAL
Regulation Number872.4565
Classification Product Code
EIL  
Date Received06/09/1987
Decision Date 07/10/1987
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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