The following data is part of a premarket notification filed by Dataview Imaging Intl., Inc. with the FDA for Image Transport Series Iii.
| Device ID | K925964 |
| 510k Number | K925964 |
| Device Name: | IMAGE TRANSPORT SERIES III |
| Classification | System, Digital Image Communications, Radiological |
| Applicant | DATAVIEW IMAGING INTL., INC. SIXTH FLOOR 1001 PENNSYLVANIA AVE. N.W. Washington, DC 20004 |
| Contact | Von Oehsen |
| Correspondent | Von Oehsen DATAVIEW IMAGING INTL., INC. SIXTH FLOOR 1001 PENNSYLVANIA AVE. N.W. Washington, DC 20004 |
| Product Code | LMD |
| CFR Regulation Number | 892.2020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-25 |
| Decision Date | 1995-02-03 |