The following data is part of a premarket notification filed by Pfizer, Inc. with the FDA for Acta-scanner 0220fs.
| Device ID | K791153 |
| 510k Number | K791153 |
| Device Name: | ACTA-SCANNER 0220FS |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | PFIZER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-06-19 |
| Decision Date | 1979-08-03 |