VERAVIEWEPOCS

System, X-ray, Extraoral Source, Digital

J. MORITA USA, INC.

The following data is part of a premarket notification filed by J. Morita Usa, Inc. with the FDA for Veraviewepocs.

Pre-market Notification Details

Device IDK073696
510k NumberK073696
Device Name:VERAVIEWEPOCS
ClassificationSystem, X-ray, Extraoral Source, Digital
Applicant J. MORITA USA, INC. 1425 K ST. N.W. SUITE 1100 Washington,  DC  20005
ContactKeith A Barritt
CorrespondentKeith A Barritt
J. MORITA USA, INC. 1425 K ST. N.W. SUITE 1100 Washington,  DC  20005
Product CodeMUH  
CFR Regulation Number872.1800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-12-31
Decision Date2008-04-08
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
04548213026432 K073696 000
04548213020447 K073696 000
04548213020430 K073696 000
04548213020423 K073696 000
04548213020416 K073696 000
04548213013708 K073696 000
04548213020379 K073696 000

Trademark Results [VERAVIEWEPOCS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERAVIEWEPOCS
VERAVIEWEPOCS
75681521 not registered Dead/Abandoned
J. MORITA MFG. CORP
1999-04-14
VERAVIEWEPOCS
VERAVIEWEPOCS
75679581 2704936 Live/Registered
J. MORITA MFG. CORP.
1999-04-12

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