The following data is part of a premarket notification filed by Philips Medical Systems North America Co. with the FDA for Allura 3d-ca, Release 1.
| Device ID | K042334 |
| 510k Number | K042334 |
| Device Name: | ALLURA 3D-CA, RELEASE 1 |
| Classification | System, Image Processing, Radiological |
| Applicant | PHILIPS MEDICAL SYSTEMS NORTH AMERICA CO. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003, MS 915 Bothell, WA 98041 -3003 |
| Contact | Lynn Harmer |
| Correspondent | Marc Mouser UNDERWRITERS LABORATORIES, INC. 2600 NW LAKE RD. Camas, WA 98607 -9526 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2004-08-30 |
| Decision Date | 2004-09-27 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838084773 | K042334 | 000 |
| 00884838059245 | K042334 | 000 |