The following data is part of a premarket notification filed by Phillips Medical Systems (cleveland) Inc. with the FDA for Philips Ct Big Bore Sliding Gantry Configuration.
| Device ID | K181797 |
| 510k Number | K181797 |
| Device Name: | Philips CT Big Bore Sliding Gantry Configuration |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Phillips Medical Systems (Cleveland) Inc. 595 Miner Road Cleveland, OH 44143 |
| Contact | Michael Chilbert |
| Correspondent | Michael Chilbert Phillips Medical Systems (Cleveland) Inc. 595 Miner Road Cleveland, OH 44143 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-07-05 |
| Decision Date | 2018-08-03 |
| Summary: | summary |