THE GNATOMET

Articulators

BAUER, CHENG & ASSOCIATES, INC.

The following data is part of a premarket notification filed by Bauer, Cheng & Associates, Inc. with the FDA for The Gnatomet.

Pre-market Notification Details

Device IDK810971
510k NumberK810971
Device Name:THE GNATOMET
ClassificationArticulators
Applicant BAUER, CHENG & ASSOCIATES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeEJP  
CFR Regulation Number872.3150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-04-09
Decision Date1981-05-05

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