The following data is part of a premarket notification filed by Siemens Medical Solutions Usa Inc. with the FDA for Somatom Flash Ds.
| Device ID | K082220 |
| 510k Number | K082220 |
| Device Name: | SOMATOM FLASH DS |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | SIEMENS MEDICAL SOLUTIONS USA INC. 51 VALLEY STREAM PARKWAY MS E50 Malvern, PA 19355 -1406 |
| Contact | Corrine Mcleod |
| Correspondent | Corrine Mcleod SIEMENS MEDICAL SOLUTIONS USA INC. 51 VALLEY STREAM PARKWAY MS E50 Malvern, PA 19355 -1406 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-06 |
| Decision Date | 2008-10-10 |
| Summary: | summary |