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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Probe, Periodontic
510(k) Number K875076
Device Name FLORIDA PROBE
Applicant
Florida Probe Corp.
1918 SW 48th Ave.
Gainesville,  FL  32608
Applicant Contact CHARLES H GIBBS,PHD
Correspondent
Florida Probe Corp.
1918 SW 48th Ave.
Gainesville,  FL  32608
Correspondent Contact CHARLES H GIBBS,PHD
Regulation Number872.4565
Classification Product Code
EIX  
Date Received12/09/1987
Decision Date 03/10/1988
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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