The following data is part of a premarket notification filed by J. Morita Usa, Inc. with the FDA for Veraviewepocs.
Device ID | K073696 |
510k Number | K073696 |
Device Name: | VERAVIEWEPOCS |
Classification | System, X-ray, Extraoral Source, Digital |
Applicant | J. MORITA USA, INC. 1425 K ST. N.W. SUITE 1100 Washington, DC 20005 |
Contact | Keith A Barritt |
Correspondent | Keith A Barritt J. MORITA USA, INC. 1425 K ST. N.W. SUITE 1100 Washington, DC 20005 |
Product Code | MUH |
CFR Regulation Number | 872.1800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-12-31 |
Decision Date | 2008-04-08 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04548213026432 | K073696 | 000 |
04548213020447 | K073696 | 000 |
04548213020430 | K073696 | 000 |
04548213020423 | K073696 | 000 |
04548213020416 | K073696 | 000 |
04548213013708 | K073696 | 000 |
04548213020379 | K073696 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VERAVIEWEPOCS 75681521 not registered Dead/Abandoned |
J. MORITA MFG. CORP 1999-04-14 |
VERAVIEWEPOCS 75679581 2704936 Live/Registered |
J. MORITA MFG. CORP. 1999-04-12 |