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 |