The following data is part of a premarket notification filed by Agfa Corp. with the FDA for Web1000.
| Device ID | K053458 |
| 510k Number | K053458 |
| Device Name: | WEB1000 |
| Classification | System, Image Processing, Radiological |
| Applicant | AGFA CORP. 455 PHILIP STREET Waterloo, Ontario, CA N2l 3x2 |
| Contact | Phil Cuscuna |
| Correspondent | Jeffrey D Rongero UNDERWRITERS LABORATORIES, INC. 12 LABORATORY DR. Research Triangle, NC 27709 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2005-12-13 |
| Decision Date | 2005-12-22 |
| Summary: | summary |