ACCOR MATRIX

Instruments, Dental Hand

ACCOR, INC.

The following data is part of a premarket notification filed by Accor, Inc. with the FDA for Accor Matrix.

Pre-market Notification Details

Device IDK790633
510k NumberK790633
Device Name:ACCOR MATRIX
ClassificationInstruments, Dental Hand
Applicant ACCOR, INC. 803 N. Front St. Suite 3 McHenry,  IL  60050
Product CodeDZN  
CFR Regulation Number872.4565 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-04-03
Decision Date1979-05-17

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