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 |