BOSWORTH DENT-ALL

Resin, Denture, Relining, Repairing, Rebasing

HARRY J. BOSWORTH CO.

The following data is part of a premarket notification filed by Harry J. Bosworth Co. with the FDA for Bosworth Dent-all.

Pre-market Notification Details

Device IDK840405
510k NumberK840405
Device Name:BOSWORTH DENT-ALL
ClassificationResin, Denture, Relining, Repairing, Rebasing
Applicant HARRY J. BOSWORTH CO. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeEBI  
CFR Regulation Number872.3760 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-01-31
Decision Date1984-05-01

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