The following data is part of a premarket notification filed by Carestream Health, Inc. with the FDA for Vita Flex Cr System With Lli.
| Device ID | K192894 |
| 510k Number | K192894 |
| Device Name: | Vita Flex CR System With LLI |
| Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
| Applicant | Carestream Health, Inc. 150 Verona Street Rochester, NY 14608 |
| Contact | Duane Gutowski |
| Correspondent | Duane Gutowski Carestream Health, Inc. 150 Verona Street Rochester, NY 14608 |
| Product Code | MQB |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-10-11 |
| Decision Date | 2020-02-18 |