The following data is part of a premarket notification filed by Imatron, Inc. with the FDA for C-ioo Mobile Cine Ct Unit.
| Device ID | K864046 |
| 510k Number | K864046 |
| Device Name: | C-IOO MOBILE CINE CT UNIT |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | IMATRON, INC. 389 OYSTER POINT BLVD. South San Francisco, CA 94080 |
| Contact | Cynthia L Haugland |
| Correspondent | Cynthia L Haugland IMATRON, INC. 389 OYSTER POINT BLVD. South San Francisco, CA 94080 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-10-16 |
| Decision Date | 1986-11-10 |