AIR-FLOW HANDY 3.0

Handpiece, Air-powered, Dental

E.M.S. ELECTRO MEDICAL SYSTEMS S.A.

The following data is part of a premarket notification filed by E.m.s. Electro Medical Systems S.a. with the FDA for Air-flow Handy 3.0.

Pre-market Notification Details

Device IDK132478
510k NumberK132478
Device Name:AIR-FLOW HANDY 3.0
ClassificationHandpiece, Air-powered, Dental
Applicant E.M.S. ELECTRO MEDICAL SYSTEMS S.A. 62 FOREST ST., STE 300 Marlborough,  MA  01752
ContactCynthia J Nolte
CorrespondentCynthia J Nolte
E.M.S. ELECTRO MEDICAL SYSTEMS S.A. 62 FOREST ST., STE 300 Marlborough,  MA  01752
Product CodeEFB  
CFR Regulation Number872.4200 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-08-08
Decision Date2014-04-11
Summary:summary

NIH GUDID Devices

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