The following data is part of a premarket notification filed by Philips Medical Systems with the FDA for Philips Viewforum 2003.
| Device ID | K032096 |
| 510k Number | K032096 |
| Device Name: | PHILIPS VIEWFORUM 2003 |
| Classification | System, Image Processing, Radiological |
| Applicant | PHILIPS MEDICAL SYSTEMS 22100 BOTHELL EVERETT HWY P.O. BOX 3003 Bothell, WA 98041 -8431 |
| Contact | Lynn T Harmer |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2003-07-08 |
| Decision Date | 2003-07-18 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838091849 | K032096 | 000 |
| 00884838081307 | K032096 | 000 |
| 00884838074804 | K032096 | 000 |
| 00884838070660 | K032096 | 000 |
| 00884838125940 | K032096 | 000 |